Laboratory and Measuring and Observing and Testing Equipment - Commodities

In this classification, 17-hydroxycorticosteroids (17-ketogenic steroids) test system connotes a device used to measure 17-hydroxycorticosteroids (17-ketogenic steroids) levels. US FDA regulates 17-hydroxycorticosteroids (17-ketogenic steroids) test system under 21 CFR 862.1385 and under FDA product code JHE.

In this classification, 17-hydroxyprogesterone test system connotes a device used to measure 17-hydroxyprogesterone levels. US FDA regulates 17-hydroxyprogesterone test system under 21 CFR 862.1395 and under FDA product code JLX.

In this classification, 17-ketosteroids test system connotes a device used to measure 17-ketosteroids levels. US FDA regulates 17-ketosteroids test system under 21 CFR 862.1430 and under FDA product code CDE.

In this classification, 2,3-diphosphoglyceric acid test system connotes a device used to measure 2,3-diphosphoglyceric acid levels. US FDA regulates 2,3-diphosphoglyceric acid test system under 21 CFR 862.1255 and under FDA product code JLY.

In this classification, a 5 hiaa tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques 5 hiaa based tumors.

In this classification, 5-hydroxyindole acetic acid/serotonin test system connotes a device used to measure 5-hydroxyindole acetic acid/serotonin levels. US FDA regulates 5-hydroxyindole acetic acid/serotonin test system under 21 CFR 862.1390 and under FDA product code CDA.

In this classification, this entry connotes a 5'-nucleotidase enzyme that is used in clinical chemistry testing.

In this classification, 5'-nucleotidase test system connotes a device used to measure 5'-nucleotidase levels. US FDA regulates 5'-nucleotidase test system under 21 CFR 862.1520 and under FDA product code CED.

In this classification, 6-phosphogluconate dehydrogenase test system connotes a device used to measure 6-phosphogluconate dehydrogenase levels. US FDA regulates 6-phosphogluconate dehydrogenase test system under 21 CFR 862.1565 and under FDA product code JND.

In this classification an abnormal hemoglobin assay is a device consisting of the reagents, apparatus, instrumentation, and controls necessary to isolate and identify abnormal genetically determined hemoglobin types US FDA regulates Abnormal hemoglobin assay under 21 CFR 864.7415 and under FDA product code GKA.

In this classification, a Acetaminophen test system is a device intended to measure Acetaminophen for clinical toxicology purposes. US FDA regulates Acetaminophen test system under 21 CFR 862.3030 and under FDA product code LDP

In this classification, this entry connotes a standardized formulation of Acetate used to conduct Anion tests.

In this classification, this entry connotes a reagent made of Acetic acid, alcohol, and toluidine blue combination used in clinical chemistry testing.

In this classification, this entry connotes a reagent made of Acid, alcohol, and decolorizing fluid used in clinical chemistry testing.

In this classification, this entry connotes a Acid phosphatase enzyme that is used in clinical chemistry testing.

In this classification, Acid phosphatase (total or prostatic) test system connotes a device used to measure Acid phosphatase (total or prostatic) levels. US FDA regulates Acid phosphatase (total or prostatic) test system under 21 CFR 862.1020 and under FDA product code CKH.

In this classification, Acinetobacter calcoaceticus serological reagents are devices used in test to identify specific Acinetobacter calcoaceticus antibodies in serum. US FDA regulates Acinetobacter calcoaceticus serological reagents under 21 CFR 866.3010 and under FDA product code GSX.

A type of equipment that generates the sound. It artificially controls the sound to use as the sound source to test the acoustic absorption, insulation of sound, residual time, penetration of sound, distribution of sound and the power of machine sound when testing the construction sound.

A standard pyrheliometer that is used to determine the correction value of the pyrheliometer. It simultaneously measures with the same environment condition of the subject pyrheliometer to determine the correction value from the difference of measurement value of both.

In this classification an activated whole blood clotting time tests is a device, used to monitor heparin therapy for the treatment of venous thrombosis or pulmonary embolism by measuring the coagulation time of whole blood US FDA regulates Activated whole blood clotting time tests under 21 CFR 864.7140 and under FDA product code JBP.

In this classification an adenosine triphosphate release assay is a device that measures the release of adenosine triphosphate (ATP) from platelets following aggregation. This measurement is made on platelet-rich plasma using a photometer and a luminescent firefly extract. Simultaneous measurements of platelet aggregation and ATP release are used to evaluate platelet function disorders US FDA regulates Adenosine triphosphate release assay under 21 CFR 864.7040 and under FDA product code KHF.

In this classification, Adenovirus serological reagents are devices used in test to identify specific Adenovirus antibodies in serum. US FDA regulates Adenovirus serological reagents under 21 CFR 866.3020 and under FDA product code GOA.

A tester that experiments the degree of an object to adhere.

In this classification, Adrenocorticotropic hormone (acth) test system connotes a device used to measure Adrenocorticotropic hormone (acth) levels. US FDA regulates Adrenocorticotropic hormone (acth) test system under 21 CFR 862.1025 and under FDA product code CKG.

In this classification, a Afp-l3% immunological test system tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Afp-l3% immunological test system based tumors. US FDA regulates Afp-l3% immunological test system under 21 CFR 866.6030 and under FDA product code OAU.

A tester that measures the specific gravity and absorption rate of thick aggregates. It is used for the analysis test of un-solidified concrete washing and it is structured of prevision specific gravity scale, steel wire for specific gravity measurement and water tank.

An instrument that is desired to measure the weight per 1 for the dried aggregates.

A tester that is designed to test the normal operation of the air purifier, filtering capability, filter replacement period, air-ventilation resistance, clean-air efficiency, dust collection and others.

When the compressed air is discharged into the air at the entrance of the container, several works can be done by using the acting force and certain sized pressure is required in accordance with the purpose of use. It is a type of device that is designed to test whether the air compressor or compressed air would maintain certain pressure.

A comparison measurement meter that uses the linear changes of air flux or pressure within the gap between the end of air-blowing nozzle and the measured surface.

In this classification, this entry connotes a Alanine amino-transferase enzyme that is used in clinical chemistry testing.

In this classification, Alanine amino transferase (alt/sgpt) test system connotes a device used to measure Alanine amino transferase (alt/sgpt) levels. US FDA regulates Alanine amino transferase (alt/sgpt) test system under 21 CFR 862.1030 and under FDA product code CKA.

In this classification, this entry connotes a substrate made of Albumin that is used in clinical chemistry testing.

In this classification, a Albumin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Albumin. US FDA regulates Albumin immunological test system under 21 CFR 866.5040 and under FDA product code DCF.

In this classification, Albumin test system connotes a device used to measure Albumin levels. US FDA regulates Albumin test system under 21 CFR 862.1035 and under FDA product code CJQ.

A meter that is designed to measure the alcoholic strength. It is the instrument that measures the Tralle scale and proof that measure the contents compared to the alcohol volume.

It is a special type of hydrometer which is used for determining the alcoholic strength of liquids.  It has a special scale marked by volume percents of an alcohol in water.

In this classification, a Alcohol test system is a device intended to measure Alcohol for clinical toxicology purposes. US FDA regulates Alcohol test system under 21 CFR 862.3040 and under FDA product code DLS

In this classification, this entry connotes a reagent made of Aldehyde urobilinogen determination used in clinical chemistry testing.

In this classification, this entry connotes an extract made of Alder used in an Immunological Allergenic test.

In this classification, this entry connotes a Aldolase enzyme that is used in clinical chemistry testing.

In this classification, Aldolase test system connotes a device used to measure Aldolase levels. US FDA regulates Aldolase test system under 21 CFR 862.1040 and under FDA product code CJC.

In this classification, Aldosterone test system connotes a device used to measure Aldosterone levels. US FDA regulates Aldosterone test system under 21 CFR 862.1045 and under FDA product code CJB.

An instrument for measuring orifices.

In this classification, this entry connotes an extract made of Alfalfa used in an Immunological Allergenic test.

A type of device that is designed to test the direction of the sideline during the flat-table surveying. It is the device to fill in on the drawing paper by setting forth the line of collimation direction that is sometimes used to measure the height difference or distance of two points.

In this classification, this entry connotes a Alkaline phosphatase enzyme that is used in clinical chemistry testing.

In this classification, this entry connotes a Alkaline phosphatase isoenzymes enzyme that is used in clinical chemistry testing.

In this classification, Alkaline phosphatase or isoenzymes test system connotes a device used to measure Alkaline phosphatase or isoenzymes levels. US FDA regulates Alkaline phosphatase or isoenzymes test system under 21 CFR 862.1050 and under FDA product code CJI.

In this classification, a Alpha-1-antichymotrypsin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Alpha-1-antichymotrypsin. US FDA regulates Alpha-1-antichymotrypsin immunological test system under 21 CFR 866.5080 and under FDA product code DFF.

In this classification, a Alpha-1-antitrypsin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Alpha-1-antitrypsin. US FDA regulates Alpha-1-antitrypsin immunological test system under 21 CFR 866.5130 and under FDA product code OBZ.

In this classification, a Alpha-1-glycoproteins immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Alpha-1-glycoproteins. US FDA regulates Alpha-1-glycoproteins immunological test system under 21 CFR 866.5420 and under FDA product code DEN.

In this classification, a Alpha-1-lipoprotein immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Alpha-1-lipoprotein. US FDA regulates Alpha-1-lipoprotein immunological test system under 21 CFR 866.5580 and under FDA product code DER.

In this classification, a Alpha-2-glycoproteins immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Alpha-2-glycoproteins. US FDA regulates Alpha-2-glycoproteins immunological test system under 21 CFR 866.5425 and under FDA product code DBC.

In this classification, a Alpha-2-macroglobulin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Alpha-2-macroglobulin. US FDA regulates Alpha-2-macroglobulin immunological test system under 21 CFR 866.5620 and under FDA product code DEB.

In this classification, a Alphafetoprotein tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Alphafetoprotein based tumors.

In this classification, a Alpha-globulin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Alpha-globulin. US FDA regulates Alpha-globulin immunological test system under 21 CFR 866.5400 and under FDA product code DCO.

In this classification, a Alpha subunit tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Alpha subunit based tumors.

A meter that measures the height above sea level. It is the device used to measure the present height at certain position or the height of the height of certain object or point on the ground.

In this classification, this entry connotes an extract made of Amaranth used in an Immunological Allergenic test.

In this classification, a Amikacin test system is a device intended to measure Amikacin for clinical toxicology purposes. US FDA regulates Amikacin test system under 21 CFR 862.3035 and under FDA product code KLP

In this classification, this entry connotes a standardized formulation of Ammonia used to conduct Anion tests.

In this classification, Ammonia test system connotes a device used to measure Ammonia levels. US FDA regulates Ammonia test system under 21 CFR 862.1065 and under FDA product code JIE.

In this classification, this entry connotes a standardized formulation of Ammonium chloride used to conduct Anion tests.

In this classification, this entry connotes a titrant of Ammonium hydroxide used as a reagent in clinical chemistry testing.

In this classification, a Amphetamine test system is a device intended to measure Amphetamine for clinical toxicology purposes. US FDA regulates Amphetamine test system under 21 CFR 862.3100 and under FDA product code DJP

A meter that is designed to measure the output of the low frequency amplifier. It is designed to change the input impedance or output level broadly. The instruction uses the rectifier type voltmeter with the scale of decibel or VU (volume unit) meter inscribed, and when using it, it is important to take the matching of impedance between the measured amplifier and the output meter.

A tester that is manufactured for the inspection of the function or capability of amplifiers in several types that are used in electric, electronic and communication circuit.

In this classification, this entry connotes a Amylase enzyme that is used in clinical chemistry testing.

In this classification, this entry connotes a Amylase isoenzyme enzyme that is used in clinical chemistry testing.

In this classification, Amylase test system connotes a device used to measure Amylase levels. US FDA regulates Amylase test system under 21 CFR 862.1070 and under FDA product code JFJ.

In this classification, a Anaerobic chamber connotes a device used as atmosphere control units designed to be used when working with oxygen sensitive materials, product containment needs, and/or general isolation control. US FDA regulates Anaerobic chamber under 21 CFR 866.2120 and under FDA product code JTM.

Gun used to anesthetize animals.

In this classification Analyte specific reagents are antibodies, both polyclonal and monoclonal, specific receptor proteins, ligands, nucleic acid sequences, and similar reagents which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens.  US FDA regulates Analyte specific reagents under 21 CFR 864.4020 and under FDA product code MVU.

A software to set up assay parameters on a clinical and diagnostic analyser

Analyzers for automated semen and sperm analysis

Replacement parts, accessories and supplies for automated semen and sperm analysis

All reagents utilized for automated semen and sperm analysis

All quality controls utilized in manual semen and sperm analysis

Reagent or solution or stain utilized for manual androgeny and fertility assessment procedures

All test kits and supplies for manual semen and sperm analysis

In this classification, Androstenedione test system connotes a device used to measure Androstenedione levels. US FDA regulates Androstenedione test system under 21 CFR 862.1075 and under FDA product code CIZ.

In this classification, Androsterone test system connotes a device used to measure Androsterone levels. US FDA regulates Androsterone test system under 21 CFR 862.1080 and under FDA product code CIY.

Equipment that is used to determine the correction value of the anemometer used to measure the wind velocity of meteorology factors.

In this classification, this entry connotes a Angiotensin converting enzyme that is used in clinical chemistry testing.

In this classification, Angiotensin converting enzyme (a.c.e.) test system connotes a device used to measure Angiotensin converting enzyme (a.c.e.) levels. US FDA regulates Angiotensin converting enzyme (a.c.e.) test system under 21 CFR 862.1090 and under FDA product code KQN.

In this classification, Angiotensin i and renin test system connotes a device used to measure Angiotensin i and renin levels. US FDA regulates Angiotensin i and renin test system under 21 CFR 862.1085 and under FDA product code CIB.

In this classification, animal and human sera are biological products, obtained from the blood of humans or other animals, that provide the necessary growth-promoting nutrients in a cell culture system. US FDA regulates Animal and human sera under 21 CFR 864.2800 and under FDA product code KIS.

Any rodent, mammal, ave, or bovine species of animal utilized for bioresearch in a laboratory setting

In this classification, this entry connotes an extract made of Ant used in an Immunological Allergenic test.

A tester that is manufactured for the inspection of capability and characteristic of the antenna that is used for receiving the wireless communication or broadcasting.

Equipment that tests the anti-biotic substances reside in dairy products, meats, and others as the chemical substance that is produced by the microbes.

Shelf Life: 36 Months Product: Anti-B Colour: Yellow Dye Used: Tartrazine The reagents will cause direct agglutination (clumping) of test red cells that carry the corresponding ABO antigen. No agglutination generally indicates absence of the corresponding ABO antigen. Lorne Monoclonal IgM ABO blood grouping reagents contain murine monoclonal antibodies diluted in a phosphate buffer containing sodium chloride, EDTA and bovine albumin. Each reagent is supplied at optimal dilution for use with slide, tube, gel card <(>&<)> microplate techniques. Reagent vials should be stored at 2 - 8ºC on receipt. Prolonged storage at temperatures outside this range may result in accelerated loss of reagent reactivity.

In this classification an antimicrobial susceptibility test disc is a device that consists of antimicrobic-impregnated paper discs used to measure by a disc-agar diffusion technique or a disc-broth elution technique the in vitro susceptibility of most clinically important bacterial pathogens to antimicrobial agents. In the disc-agar diffusion technique, bacterial susceptibility is ascertained by directly measuring the magnitude of a zone of bacterial inhibition around the disc on an agar surface. The disc-broth elution technique is associated with an automated rapid susceptibility test system and employs a fluid medium in which susceptibility is ascertained by photometrically measuring changes in bacterial growth resulting when antimicrobial material is eluted from the disc into the fluid medium. Test results are used to determine the antimicrobial agent of choice in the treatment of bacterial diseases US FDA regulates Antimicrobial susceptibility test disc under 21 CFR 866.1620 and under FDA product code JTN.

In this classification an antimicrobial susceptibility test powder is a device that consists of an antimicrobial drug powder packaged in vials in specified amounts and intended for use in clinical laboratories for determining in vitro susceptibility of bacterial pathogens to these therapeutic agents. Test results are used to determine the antimicrobial agent of choice in the treatment of bacterial diseases US FDA regulates Antimicrobial susceptibility test powder under 21 CFR 866.1640 and under FDA product code MJA.

In this classification, a Antimitochondrial antibody immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Antimitochondrial antibody. US FDA regulates Antimitochondrial antibody immunological test system under 21 CFR 866.5090 and under FDA product code DBM.

In this classification, a Antimony test system is a device intended to measure Antimony for clinical toxicology purposes. US FDA regulates Antimony test system under 21 CFR 862.3110 and under FDA product code DNE

In this classification, a Antinuclear antibody immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Antinuclear antibody. US FDA regulates Antinuclear antibody immunological test system under 21 CFR 866.5100 and under FDA product code LSW.

In this classification, a Antiparietal antibody immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Antiparietal antibody. US FDA regulates Antiparietal antibody immunological test system under 21 CFR 866.5110 and under FDA product code MLE.

In this classification, a Anti-saccharomyces cerevisiae(s. cerevisiae) antibody (asca) test systems is a device that consists of the reagents used to identify by immunochemical techniques Anti-saccharomyces cerevisiae(s. cerevisiae) antibody (asca). US FDA regulates Anti-saccharomyces cerevisiae(s. cerevisiae) antibody (asca) test systems under 21 CFR 866.5785 and under FDA product code NBT.

In this classification, a Antismooth muscle antibody immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Antismooth muscle antibody. US FDA regulates Antismooth muscle antibody immunological test system under 21 CFR 866.5120 and under FDA product code NJF.

In this classification an antithrombin III assay is a device that is used to determine the plasma level of antithrombin III (a substance which acts with the anticoagulant heparin to prevent coagulation). This determination is used to monitor the administration of heparin in the treatment of thrombosis US FDA regulates Antithrombin iii assay under 21 CFR 864.7060 and under FDA product code JPE.

In this classification, this entry connotes an extract made of Apricot used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Arbor vitae used in an Immunological Allergenic test.

In this classification, Arizonagenus serological reagents are devices used in test to identify specific Arizonagenus antibodies in serum. US FDA regulates Arizonagenus serological reagents under 21 CFR 866.3035 and under FDA product code GTE.

A type of device that absorbs the harmful toxic gas and releases out the gas and others generated from the chemical or physical reaction at the laboratory or research center to outside of building and others through the pipes.

A tester that is designed to test for any malfunctioning of the lightning arrester.

Arsenic is the critically toxic compound for human body even for a small volume and it is the gray white-colored element is heated to sublime to generate compound with very strong chemical. This is a type of device that detects arsenic.

In this classification, a Arsenic test system is a device intended to measure Arsenic for clinical toxicology purposes. US FDA regulates Arsenic test system under 21 CFR 862.3120 and under FDA product code DNZ

Syringe or capillary tube and the mixing fleas, magnets, stoppers and/or the accompanying phlebotomy supplies utilized for the collection of capillary or arterial blood gas specimens

In this classification, this entry connotes an extract made of Artichoke used in an Immunological Allergenic test.

In this classification, Ascorbic acid test system connotes a device used to measure Ascorbic acid levels. US FDA regulates Ascorbic acid test system under 21 CFR 862.1095 and under FDA product code JMA.

In this classification, this entry connotes an extract made of Ash used in an Immunological Allergenic test.

In this classification, this entry connotes a Aspartate amino-transferase enzyme that is used in clinical chemistry testing.

In this classification, Aspartate amino transferase (ast/sgot) test system connotes a device used to measure Aspartate amino transferase (ast/sgot) levels. US FDA regulates Aspartate amino transferase (ast/sgot) test system under 21 CFR 862.1100 and under FDA product code CIT.

In this classification, this entry connotes an extract made of Aspen used in an Immunological Allergenic test.

In this classification, Aspergillus genus serological reagents are devices used in test to identify specific Aspergillus genus antibodies in serum. US FDA regulates Aspergillus genus serological reagents under 21 CFR 866.3040 and under FDA product code JWT.

A tester that measures the softening point of the asphalt with the ring and ball method.

Pipette that is unplugged, ungraduated and sterile, utilized for aspirating liquids by vacuum suction methodology

In this classification, this entry connotes a colorimetric standard that incorporates the ASTM Color Index.

Accessories adding speed and a better sample identification to an autosampler

In this classification an atomic absorption spectrophotometer for clinical use is a device intended to identify and measure elements and metals (e.g., lead and mercury) in human specimens. The metal elements are identified according to the wavelength and intensity of the light that is absorbed when the specimen is converted to the atomic vapor phase US FDA regulates Atomic absorption spectrophotometer for clinical use under 21 CFR 862.2850 and under FDA product code JXR.

A type of telescope that is used in the measurement of the micro-angle. The focus glass inscribed with the cross mark line or angle scale is placed on the focusing part of the objective lens. For the optical axis on the front of the objective lens, it is placed vertically to form on the same focusing part by the plane reflection glass for image. It measures the straightness, flatness, parallelism, micro-angle and others and is used for inspecting machine tool and angle gauge.

In this classification, an automated blood cell diluting apparatus is a fully automated or semi-automated device used to make appropriate dilutions of a blood sample for further testing. US FDA regulates Automated blood cell diluting apparatus under 21 CFR 864.5240 and under FDA product code GKH.

In this classification, an automated blood cell separator is a device that uses a centrifugal or filtration separation principle to automatically withdraw whole blood from a donor, separate the whole blood into blood components, collect one or more of the blood components, and return to the donor the remainder of the whole blood and blood components. US FDA regulates Automated blood cell separator under 21 CFR 864.9245 and under FDA product code GKT.

Automated system for incubating and processing blood cultures

Replacement parts, accessories and supplies for automated blood culture system

Reagent or media enrichment and supplement utilized for automated blood culture system

In this classification, an automated blood grouping and antibody test system is a device used to group erythrocytes (red blood cells) and to detect antibodies to blood group antigens. US FDA regulates Automated blood grouping and antibody test system under 21 CFR 864.9175 and under FDA product code KSZ.

In this classification, an automated cell counter is a fully-automated or semi-automated device used to count red blood cells, white blood cells, or blood platelets using a sample of the patient's peripheral blood (blood circulating in one of the body's extremities, such as the arm). US FDA regulates Automated cell counter under 21 CFR 864.5200 and under FDA product code GKL.

In this classification, an automated cell-locating device is a device used to locate blood cells on a peripheral blood smear, allowing the operator to identify and classify each cell according to type. US FDA regulates Automated cell-locating device under 21 CFR 864.5260 and under FDA product code JOY.

In this classification, an automated cell-washing centrifuge for immuno-hematology is a device used to separate and prepare cells and sera for further in vitro diagnostic testing. US FDA regulates Automated cell-washing centrifuge for immuno-hematology under 21 CFR 864.9285 and under FDA product code KSN.

In this classification, a Automated colony counter connotes a device used for the automated counting colonies of bacteria growing in a culture US FDA regulates Automated colony counter under 21 CFR 866.2170 and under FDA product code KZB.

In this classification, an automated Coombs test system is a device used to detect and identify antibodies in patient sera or antibodies bound to red cells. The Coombs test is used for the diagnosis of hemolytic disease of the newborn, and autoimmune hemolytic anemia. The test is also used in cross matching and in investigating transfusion reactions and drug-induced red cell sensitization. US FDA regulates Automated coombs test systems under 21 CFR 864.9300 and under FDA product code KSM.

In this classification, an automated differential cell counter is a device used to identify one or more of the formed elements of the blood. The device may also have the capability to flag, count, or classify immature or abnormal hematopoietic cells of the blood, bone marrow, or other body fluids. US FDA regulates Automated differential cell counter under 21 CFR 864.5220 and under FDA product code GKZ.

In this classification, Automated fluorescencein situhybridization (fish) enumeration systems connotes a device that consists of an automated scanning microscope, image analysis system, and customized software applications for FISH assays. This device is intended for in vitro diagnostic use with FISH assays as an aid in the detection, counting and classification of cells based on recognition of cellular color, size, and shape, and in the detection and enumeration of FISH signals in interphase nuclei of formalin-fixed, paraffin-embedded human tissue specimens. US FDA regulates Automated fluorescencein situhybridization (fish) enumeration systems under 21 CFR 866.4700 and under FDA product code NTH.

In this classification, an automated hematocrit instrument is a fully automated or semi-automated device which may or may not be part of a larger system. This device measures the packed red cell volume of a blood sample to distinguish normal from abnormal states, such as anemia and erythrocytosis (an increase in the number of red cells). US FDA regulates Automated hematocrit instrument under 21 CFR 864.5600 and under FDA product code GKF.

In this classification, an automated hemoglobin system is a fully automated or semi-automated device which may or may not be part of a larger system. The generic type of device consists of the reagents, calibrators, controls, and instrumentation used to determine the hemoglobin content of human blood. US FDA regulates Automated hemoglobin system under 21 CFR 864.5620 and under FDA product code GKR.

In this classification, an automated heparin analyzer is a device used to determine the heparin level in a blood sample by mixing the sample with protamine (a heparin-neutralizing substance) and determining photometrically the onset of air-activated clotting. The analyzer also determines the amount of protamine necessary to neutralize the heparin in the patient's circulation. US FDA regulates Automated heparin analyzer under 21 CFR 864.5680 and under FDA product code JOX.

Automated systems utlizing high performance chromatography HPLC methodology for biochemical quantitation

Replacement parts and accessories utilized for high performance chromatography HPLC automated testing systems

Reagent or kit utilized for biochemical quantitation by automated high performance chromatography HPLC analysis

Replacment parts and accessories utilized on automated liquid handling and diluter systems

In this classification, a Automated medium dispensing and stacking device connotes a device used  for medical purposes to dispense a microbiological culture medium into petri dishes and then mechanically stack the petri dishes. US FDA regulates Automated medium dispensing and stacking device under 21 CFR 866.2440 and under FDA product code JTB.

An automated processing system that inoculates and streaks universal specimen types and sources onto plated and tubed media

Automated microscope labeling system and its accessories and supplies

A system that captures, analyzes and/or archives product images to determine the presence or absence of defects.

In this classification, an automated platelet aggregation system is a device used to determine changes in platelet shape and platelet aggregation following the addition of an aggregating reagent to a platelet-rich plasma. US FDA regulates Automated platelet aggregation system under 21 CFR 864.5700 and under FDA product code JOZ.

Analyzer system and software designed to manage laboratory assay quality control data, providing a mechanism to automate, centralize, standardize and implement QC processes necessary for accreditation and cost management.

In this classification, an automated sedimentation rate device is an instrument that measures automatically the erythrocyte sedimentation rate in whole blood. Because an increased sedimentation rate indicates tissue damage or inflammation, the erythrocyte sedimentation rate device is useful in monitoring treatment of a disease. US FDA regulates Automated sedimentation rate device under 21 CFR 864.5800 and under FDA product code GKB.

In this classification, an automated slide spinner is a device that prepares automatically a blood film on a microscope slide using a small amount of peripheral blood (blood circulating in one of the body's extremities, such as the arm. US FDA regulates Automated slide spinner under 21 CFR 864.5850 and under FDA product code GKJ.

In this classification an automated slide stainer uses specific labeled antibodies, conjugated enzymes, and peroxidase to individual slides, which are applied in a specific predetermined order. These reagents are applied in small, controlled volumes to the tissue on the slides; slides are not immersed in the reagents. US FDA regulates Automated slide stainer under 21 CFR 864.3800 and under FDA product code KPA.

Automated tissue cassette labelers and their accessories and supplies

In this classification an automated tissue processor is a device that without manual intervention prepares very thin, high quality sections (slices) mounted on glass slides and appropriately stained to demonstrate normal and abnormal structures. US FDA regulates Automated tissue processor under 21 CFR 864.3875 and under FDA product code IEO.

In this classification an automated urinalysis system is a device intended to measure certain of the physical properties and chemical constituents of urine by procedures that duplicate manual urinalysis systems. This device is used in conjunction with certain materials to measure a variety of urinary analytes US FDA regulates Automated urinalysis system under 21 CFR 862.2900 and under FDA product code KQO.

Automated system which utilizes a hands free torque technique to decap and recap tubes or vials while retaining reagent and sample integrity

In this classification, a Automated zone reader connotes a mechanical device intended for medical purposes to measure zone diameters of microbial growth inhibition (or exhibition), such as those observed on the surface of certain culture media used in disc-agar diffusion antimicrobial susceptibility tests. The device aids in decision-making respecting the treatment of disease US FDA regulates Automated zone reader under 21 CFR 866.2850 and under FDA product code KZK.

A type of scale that is used to pack by measuring for certain level of quantity --volume for a pack-- for cigarette comes out of production from the plant.

A scale that selects properties automatically for each weight with the pre-determined standard.

Equipment that enables the capability inspection on each sensing element of the automatic weather system and check the data logger.

Film used for chemiluminescent detection of protein and nucleic acid samples that have been labeled with radioisotopes

Scales to capture weights of large cargo loads or baggage scales to keep inbound and outbound passengers

In this classification, a balanced salt solution or formulation is a defined mixture of salts and glucose in a simple medium. This device is included as a necessary component of most cell culture systems. This media component controls for pH, osmotic pressure, energy source, and inorganic ions. US FDA regulates Balanced salt solutions or formulations under 21 CFR 864.2875 and under FDA product code KIP.

In this classification, a Barbiturate test system is a device intended to measure Barbiturate for clinical toxicology purposes. US FDA regulates Barbiturate test system under 21 CFR 862.3150 and under FDA product code DMF

In this classification, this entry connotes an extract made of Barley used in an Immunological Allergenic test.

Equipment that is used to determine the correction value of the scale inscribed on the barometer by changing to pressure in the chamber to 950hPa, 990hPa, 1010hPa and 1040hPa.

A facility that closes and opens the circuit by the change of air pressure. The circuit of measurement sensor other than the temperature, humidity, and air pressure of radiosonde is used to make automatic connection to the sequential transmitter in accordance with the reduction of the air pressure following the increase of the device.

In this classification, this entry connotes an extract made of Bass used in an Immunological Allergenic test.

An apparatus that experiments bending, deformation, twisting, stress of beam and others in accordance with the shape, structure, support method and others of various beams.

In this classification, this entry connotes an extract made of Bean used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Bee used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Beech used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Beet used in an Immunological Allergenic test.

A tester that is designed to test the characteristics of V belt that is used for delivering the vehicle power and general power.

In this classification, a Bence-jones proteins immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Bence-jones proteins. US FDA regulates Bence-jones proteins immunological test system under 21 CFR 866.5150 and under FDA product code CZQ.

Ice buckets and containers used for chilling specimens on the workbench

Racks for the storage and organization of reagent bottles utilized at the workbench

In this classification, this entry connotes an extract made of Bent grassused in an Immunological Allergenic test.

In this classification, a Benzodiazepine test system is a device intended to measure Benzodiazepine for clinical toxicology purposes. US FDA regulates Benzodiazepine test system under 21 CFR 862.3170 and under FDA product code JXM

In this classification, a Beta-2-glycoprotein iii immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Beta-2-glycoprotein iii. US FDA regulates Beta-2-glycoprotein iii immunological test system under 21 CFR 866.5440 and under FDA product code DDK.

In this classification, a Beta-2-glycoprotein i immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Beta-2-glycoprotein i. US FDA regulates Beta-2-glycoprotein i immunological test system under 21 CFR 866.5430 and under FDA product code DDN.

In this classification, a Beta-2-microglobulin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Beta-2-microglobulin. US FDA regulates Beta-2-microglobulin immunological test system under 21 CFR 866.5630 and under FDA product code JZG.

In this classification, a Beta2-microglobulin tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Beta2-microglobulin based tumors.

In this classification, a Beta-globulin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Beta-globulin. US FDA regulates Beta-globulin immunological test system under 21 CFR 866.5160 and under FDA product code DCJ.

In this classification, Beta-glucan serological assays are devices used in test to identify specific Beta-glucan serological assays antibodies in serum. US FDA regulates Beta-glucan serological assays under 21 CFR 866.3050 and under FDA product code NQZ.

In this classification a beta or gamma counter for clinical use is a device intended to detect and count beta or gamma radiation emitted by clinical samples. Clinical samples are prepared by addition of a radioactive reagent to the sample. These measurements are useful in the diagnosis and treatment of various disorders US FDA regulates Beta or gamma counter for clinical use under 21 CFR 862.2320 and under FDA product code JJJ.

Highly absorbent paper for drying microscope slides and coverslips

In this classification, Bicarbonate/carbon dioxide test system connotes a device used to measure Bicarbonate/carbon dioxide levels. US FDA regulates Bicarbonate/carbon dioxide test system under 21 CFR 862.1160 and under FDA product code CIE.

In this classification, this entry connotes a titrant of Biiodate used as a reagent in clinical chemistry testing.

In this classification, this entry connotes a substrate made of Bile acids that is used in clinical chemistry testing.

In this classification, this entry connotes a substrate made of Bilirubin that is used in clinical chemistry testing.

In this classification, Bilirubin (total and unbound) in the neonate test system connotes a device used to measure Bilirubin (total and unbound) in the neonate levels. US FDA regulates Bilirubin (total and unbound) in the neonate test system under 21 CFR 862.1113 and under FDA product code MQM.

In this classification, Bilirubin (total or direct) test system connotes a device used to measure Bilirubin (total or direct) levels. US FDA regulates Bilirubin (total or direct) test system under 21 CFR 862.1110 and under FDA product code CIG.

A machine like a computer which counts in binary.

A meter that measures the oxygen volume that is required for the aerobic bacteria to secrete the organic substance within certain time.

A device used for high velocity injection of DNA-coated fragments directly into host tissues, cells, or organelles, resulting in the transformation of virtually any diverse cell target

An enclosed workspace which utilizes HEPA filtering for both intake and exhaust ventilation, which may or may not function through laminar flow, which is divided into biological safety classes and which is used in the laboratory for safely working with materials contaminated with, or which could be potentially contaminated with, pathogens

Automated system which applies a magnetic force on particles within a solution in order to separate molecules, specific proteins, cells or nucleic acids within in vitro and in vivo scenarios

Replacement parts and accessories utilized on magnetic bioseparation analyzers

Single use container or bag which is utilized for the safe and protected manufacturing, packaging, intermediate storage and transport of bioprocessing medias, buffers, water for injection and other biological products used in molecular biology platforms

In this classification, Biotinidase test system connotes a device used to measure Biotinidase levels. US FDA regulates Biotinidase test system under 21 CFR 862.1118 and under FDA product code NAK.

In this classification, this entry connotes an extract made of Birch used in an Immunological Allergenic test.

In this classification, a Bladder tumor tissue antigen tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Bladder tumor tissue antigen based tumors.

A tester that measures on how many shots can be made by using the blasting machine.

In this classification, Blastomyces dermatitidis serological reagents are devices used in test to identify specific Blastomyces dermatitidis antibodies in serum. US FDA regulates Blastomyces dermatitidis serological reagents under 21 CFR 866.3060 and under FDA product code LSH.

In this classification, Bleeding time device connotes a device used to usually employing two spring-loaded blades, that produces two small incisions in the patient's skin. The length of time required for the bleeding to stop is a measure of the effectiveness of the coagulation system, primarily the platelets. US FDA regulates Bleeding time device under 21 CFR 864.6100 and under FDA product code JCA.

In this classification, a no electromagnetic blood and plasma warming device is a device that warms blood or plasma, by means other than electromagnetic radiation, prior to administration. US FDA regulates Blood and plasma warming device under 21 CFR 864.9205 and under FDA product code KZL.

All analyzers utilized for blood component therapy collection, apheresis and processing

Replacement parts, tubing sets, accessories and supplies for automated blood component therapy collection and processing

In this classification, a blood bank centrifuge for in vitro diagnostic use is a device used only to separate blood cells for further diagnostic testing. US FDA regulates Blood bank centrifuge for in vitro diagnostic use under 21 CFR 864.9275 and under FDA product code KSO.

Baths for the controlled and rapid thawing of fresh frozen plasma for transfusion

In this classification, Blood bank supplies are general purpose devices intended for in vitro use in blood banking. This generic type of device includes products such as blood bank pipettes, blood grouping slides, blood typing tubes, blood typing racks, and cold packs for antisera reagents. US FDA regulates Blood bank supplies under 21 CFR 864.9050 and under FDA product code KSS.

Monitor or meter utilized for point of care whole blood bilirubin quantitation

Replacement parts and accessories for point of care whole blood bilirubin test monitor or meter

In this classification a blood cell diluent is a device used to dilute blood for further testing, such as blood cell counting US FDA regulates Blood cell diluent under 21 CFR 864.8200 and under FDA product code GIF.

Point of care rapid test meter for the measurement of single or multiple parameter chemistry analytes in whole blood.

Point of care rapid test meter for the measurement of single or multiple parameter hemostasis analytes in whole blood

In this classification, this entry conforms with blood collection needle holders as validated against FDA product codes

Container and/or rack for the organization and dispensing of blood collection tubes in the phlebotomy area

In this classification, this commodity indicates a product used as a blood collection tubing stripper-sealer-cutter during a medical procedure in a medical setting. Most nations, for tariff and trade purposes, schedule these products under HS 901839.

Kit used to collect blood culture specimens that includes all venipuncture supplies and/or antimicrobial skin cleansing preparations, and/or is inclusive with blood culture bottles

Closed tube piercing sampler that dispenses blood drops for the preparation of peripheral blood smears

In this classification, Blood gases (pco2, po2) and blood ph test system connotes a device used to measure Blood gases (pco2, po2) and blood ph levels. US FDA regulates Blood gases (pco2, po2) and blood ph test system under 21 CFR 862.1120 and under FDA product code CHL.

In this classification, a blood grouping view box is a device with a glass or plastic viewing surface, which may be illuminated and heated, that is used to view cell reactions in antigen-antibody testing. US FDA regulates Blood grouping view box under 21 CFR 864.9185 and under FDA product code KSY.

In this classification, blood group substances of nonhuman origin for in vitro diagnostic use are materials, such as blood group specific substances prepared from nonhuman sources (e.g., pigs, cows, and horses) used to detect, identify, or neutralize antibodies to various human blood group antigens. US FDA regulates Blood group substances of nonhuman origin for in vitro diagnostic use under 21 CFR 864.9160 and under FDA product code KSX.

Monitors or meters ultized for point of care whole blood lead analysis

Replacment parts and accessories for whole blood lead test meters

In this classification, a blood mixing device is a device intended for medical purposes that is used to mix blood or blood components by agitation. A blood weighing device is a device intended for medical purposes that is used to weigh blood or blood components as they are collected. US FDA regulates Blood mixing devices and blood weighing devices under 21 CFR 864.9195 and under FDA product code KSQ.

In this classification, Blood specimen collection device connotes a device used to measure Blood specimen collection device levels. US FDA regulates Blood specimen collection device under 21 CFR 862.1675 and under FDA product code PJE.

In this classification, a blood storage refrigerator and a blood storage freezer are devices intended for medical purposes that are used to preserve blood and blood products by storing them at cold or freezing temperatures. US FDA regulates Blood storage refrigerator and blood storage freezer under 21 CFR 864.9700 and under FDA product code KSE.

Boots and racks used to storage blood units in blood bank refrigerators

Irreversible strips for monitoring blood unit temperature integrity

High temperature unit for the aseptic sealing of blood donor unit tubing.

Specialized system including software utilized for tracking blood component therapy distribution and utilization

In this classification, a blood volume measuring device is a manual, semi automated, or automated system that is used to calculate the red cell mass, plasma volume, and total blood volume. US FDA regulates Blood volume measuring device under 21 CFR 864.5950 and under FDA product code JWO.

In this classification, Blood volume test system connotes a device used to measure Blood volume levels. US FDA regulates Blood volume test system under 21 CFR 862.1130 and under FDA product code JKP.

In this classification, this entry connotes an extract made of Bluegrass used in an Immunological Allergenic test.

A tester that is designed to measure and test the extreme force and strength.

In this classification, this entry connotes a reagent made of Bone decalcifying solutions that is used in clinical chemistry testing.

In this classification, Bordetella genus serological reagents are devices used in test to identify specific Bordetella genus antibodies in serum. US FDA regulates Bordetella genus serological reagents under 21 CFR 866.3065 and under FDA product code GOT.

In this classification, this entry connotes a standardized formulation of Boron used to conduct Anion tests.

In this classification a Bothrops atrox reagent is a device made from snake venom and used to determine blood fibrinogen levels to aid in the evaluation of disseminated intravascular coagulation (non localized clotting in the blood vessels) in patients receiving heparin therapy (the administration of the anticoagulant heparin in the treatment of thrombosis) or as an aid in the classification of dysfibrinogenemia (presence in the plasma of functionally defective fibrinogen) US FDA regulates Bothrops atrox reagent under 21 CFR 864.8100 and under FDA product code JCO.

Bottled or tubed agarose media forumulated for the general and selective growth of yeast

Broth media utilized for the general or selective growth and differentiation of aerobic and anaerobic bacteria

Broth media utilized for the general or selective growth and differentiation of yeast

A sterile preparation of purified water or normal saline utilized in diverse routine microbiological applications

A tester that measures the signal for brake and other condition to determine for any problems. It is the tester that determines if the functions of running prevention, idle rotation prevention and others operate normally.

In this classification, a Breast milk immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Breast milk. US FDA regulates Breast milk immunological test system under 21 CFR 866.5170 and under FDA product code DGM.

In this classification, a Breath-alcohol test system is a device intended to measure Breath-alcohol for clinical toxicology purposes. US FDA regulates Breath-alcohol test system under 21 CFR 862.3050 and under FDA product code DJZ

In this classification, a Breath nitric oxide test system is a device intended to measure Breath nitric oxide for clinical toxicology purposes. US FDA regulates Breath nitric oxide test system under 21 CFR 862.3080 and under FDA product code MXA

In this classification, this entry connotes a titrant of Bromate-bromide used as a reagent in clinical chemistry testing.

In this classification, this entry connotes a standardized formulation of Bromate used to conduct Anion tests.

In this classification, this entry connotes an extract made of Brome used in an Immunological Allergenic test.

In this classification, this entry connotes a standardized formulation of Bromide used to conduct Anion tests.

In this classification, Brucella genus serological reagents are devices used in test to identify specific Brucella genus antibodies in serum. US FDA regulates Brucella genus serological reagents under 21 CFR 866.3085 and under FDA product code GSO.

In this classification, B-type natriuretic peptide test system connotes a device used to measure B-type natriuretic peptide levels. US FDA regulates B-type natriuretic peptide test system under 21 CFR 862.1117 and under FDA product code NBC.

In this classification, this entry connotes an extract made of Bunch used in an Immunological Allergenic test.

A tester that is designed to measure and test the destruction pressure within the permitted range of container that takes certain pressure, such as liquefied petroleum gas (LPG) container, glass bottle for carbonated drink and others.

A tester that measures the pressure when the specimen is broken with the pressure applied to the thin-plate shaped material, such as paper, fiber, vinyl film, medical leather and others.

In this classification, this entry connotes an extract made of Cabbage used in an Immunological Allergenic test.

A manual device that is used to measure with certain precision the distance between a source and a movable object by way of a wire or cable connecting them.

In this classification, Calcitonin test system connotes a device used to measure Calcitonin levels. US FDA regulates Calcitonin test system under 21 CFR 862.1140 and under FDA product code JKR.

In this classification, Calcium test system connotes a device used to measure Calcium levels. US FDA regulates Calcium test system under 21 CFR 862.1145 and under FDA product code JFP.

In this classification, this entry connotes a titrant of Calcium used as a reagent in clinical chemistry testing.

In this classification a calculator/data processing module for clinical use is an electronic device intended to store, retrieve, and process laboratory data US FDA regulates Calculator/data processing module for clinical use under 21 CFR 862.2100 and under FDA product code JQP.

The calibration column is designed specifically for use in determining flow rates of chemical metering pumps Pump flow rate verification on periodic basis or after maintenance is important to system accuracy.

A calibrated reference thermometer, certified by the National Institute of Standards and Technology, NIST, that maintains metrologic traceability, and that is utilized to calibrate or verify that any other thermometer will measure within that specific temperature range in which the thermometer is designed to operate

In this classification a calibrator for cell indices is a device that approximates whole blood or certain blood cells and that is used to set an instrument intended to measure mean cell volume (MCV), mean corpuscular hemoglobin (MCH), and mean corpuscular hemoglobin concentration (MCHC), or other cell indices US FDA regulates Calibrator for cell indices under 21 CFR 864.8150 and under FDA product code KRX.

In this classification a calibrator for hemoglobin or hematocrit measurement is a device that approximates whole blood, red blood cells, or a hemoglobin derivative and that is used to set instruments intended to measure hemoglobin, the hematocrit, or both. It is a material whose characteristics have been precisely and accurately determined US FDA regulates Calibrator for hemoglobin or hematocrit measurement under 21 CFR 864.8165 and under FDA product code KRZ.

In this classification a calibrator for platelet counting is a device that resembles platelets in plasma or whole blood and that is used to set a platelet counting instrument. It is a suspension of particles or cells whose size, shape concentration, and other characteristics have been precisely and accurately determined US FDA regulates Calibrator for platelet counting under 21 CFR 864.8175 and under FDA product code KRY.

In this classification a calibrator for red cell and white cell counting is a device that resembles red or white blood cells and that is used to set instruments intended to count red cells, white cells, or both. It is a suspension of particles or cells whose size, shape, concentration, and other characteristics have been precisely and accurately determined US FDA regulates Calibrator for red cell and white cell counting under 21 CFR 864.8185 and under FDA product code KSA.

In this classification, Calibrator IVD device connotes a device used to measure Calibrator IVD device levels. US FDA regulates Calibrator IVD device under 21 CFR 862.1150 and under FDA product code JIX.

A soil tester that is used to determine the California bearing ratio of the subgrade soil by the penetration method in order to determine the bearing capacity of subgrade or roadbed.

In this classification, Campylobacter fetus serological reagents are devices used in test to identify specific Campylobacter fetus antibodies in serum. US FDA regulates Campylobacter fetus serological reagents under 21 CFR 866.3110 and under FDA product code GSP.

In this classification, this entry connotes an extract made of Canary grass used in an Immunological Allergenic test.

In this classification, a Cancer antigen 125 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Cancer antigen 125 based tumors.

In this classification, a Cancer antigen 15-3 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Cancer antigen 15-3 based tumors.

In this classification, a Cancer antigen 195 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Cancer antigen 195 based tumors.

In this classification, a Cancer antigen 19-9 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Cancer antigen 19-9 based tumors.

In this classification, a Cancer antigen 242 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Cancer antigen 242 based tumors.

In this classification, a Cancer antigen 27.29 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Cancer antigen 27.29 based tumors.

In this classification, a Cancer antigen 50 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Cancer antigen 50 based tumors.

In this classification, a Cancer antigen 549 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Cancer antigen 549 based tumors.

In this classification, a Cancer antigen 72-4 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Cancer antigen 72-4 based tumors.

In this classification, a Cancer antigens tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Cancer antigens based tumors.

In this classification, a Cancer associated serum antigen tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Cancer associated serum antigen based tumors.

In this classification, a Cannabinoid test system is a device intended to measure Cannabinoid for clinical toxicology purposes. US FDA regulates Cannabinoid test system under 21 CFR 862.3870 and under FDA product code LAT

A tester that tests the electrostatic capacity, duration, discharge characteristic and others to find out the abnormality of the condenser. It has the different measurement range in accordance with the condenser capacity.

In this classification, Capillary blood collection tube connotes a device used to as a plain or heparinized glass tube of very small diameter used to collect blood by capillary action. US FDA regulates Capillary blood collection tube under 21 CFR 864.6150 and under FDA product code GIO.

A mechanism designed to pull thin wall glass capillaries to generate tubes, pipettes or needles suitable for cell culture growth, seeding, in vivo microscopic imaging and/or microinjection studies

A tester that measures the capillary tube pressure of air and water, water and oil, or 3 or more fluids. This equipment is equipped with the mercury pump, and it measures the pressure from the time mercury smears into the sample and the pressure when no more smearing can be made in graph.

A type of device that is used for culturing the bacilli or tissue that cannot be cultured without the carbon dioxide CO2 gas when culturing the bacilli or tissue at the hospital bacilli laboratory or other research institute.

In this classification, a Carbonic anhydrase b and c immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Carbonic anhydrase b and c. US FDA regulates Carbonic anhydrase b and c immunological test system under 21 CFR 866.5200 and under FDA product code KTK.

An instrument used to measure carbon monoxide(CO) in gas.

In this classification, a Carbon monoxide test system is a device intended to measure Carbon monoxide for clinical toxicology purposes. US FDA regulates Carbon monoxide test system under 21 CFR 862.3220 and under FDA product code JKT

In this classification a carboxyhemoglobin assay is a device used to determine the carboxyhemoglobin (the compound formed when hemoglobin is exposed to carbon monoxide) content of human blood as an aid in the diagnosis of carbon monoxide poisoning. This measurement may be made using methods such as spectroscopy, colorimetry, spectrophotometry, and gasometry US FDA regulates Carboxyhemoglobin assay under 21 CFR 864.7425 and under FDA product code LGL.

In this classification, a Carcinoembryonic antigen tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Carcinoembryonic antigen based tumors.

In this classification, Cardiac allograft gene expression profiling test system connotes a device used to measure Cardiac allograft gene expression profiling levels. US FDA regulates Cardiac allograft gene expression profiling test system under 21 CFR 862.1163 and under FDA product code OJQ.

Monitor or meter utilized for point of care whole blood cardiac markers analysis

Replacment parts and accessories utilized for point of care whole blood cardiac marker test monitor or meter

Quality control reagents used in hospital laboratory cardiac marker testing.

Reagents used in hospital laboratory cardiac marker testing.

Cardiac marker test kits used in hospital laboratory cardiac marker testing.

In this classification, this entry connotes an extract made of Casein used in an Immunological Allergenic test.

In this classification, Catecholamines (total) test system connotes a device used to measure Catecholamines (total) levels. US FDA regulates Catecholamines (total) test system under 21 CFR 862.1165 and under FDA product code CHT.

In this classification, a Cathepsin-d tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Cathepsin-d based tumors.

It is the structure that is installed horizontally with the telescope that moves up and down the metal column that is erected vertically. The vertical pillar uses the tri-pot and is attached level to vertically adjust and the telescope adjusts levelness with the level attached to the upper part.

In this classification, this entry connotes an extract made of Cattail used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Cattle epithelium used in an Immunological Allergenic test.

A type of device that displays the electromagnetic wave or electric oscillation in general.

In this classification, this entry connotes an extract made of Cedar used in an Immunological Allergenic test.

A meter that is designed to measure and record the height of the cloud floor. There are optical method and electric wave method, and it is consisted of three parts; light, electric wave launcher and, receiver and recorder. The part combined with the receiver and recorder is referred to as the detector.

In this classification, cell and tissue culture supplies and equipment are devices that are used to examine, propagate, nourish, or grow cells and tissue cultures. These include such articles as slide culture chambers, perfusion and roller apparatus, cell culture suspension systems, and tissue culture flasks, disks, tubes, and roller bottles. US FDA regulates Cell and tissue culture supplies and equipment under 21 CFR 864.2240 and under FDA product code KIY.

Porous glass capillary tubes able to contain ultra micro volumes of cell culture suspensions for growth, seeding, in vivo microscopic imaging, and/or microinjection into living cells

In this classification, cell-freezing apparatus and reagents for in vitro diagnostic use are devices used to freeze human red blood cells for in vitro diagnostic use. US FDA regulates Cell-freezing apparatus and reagents for in vitro diagnostic use under 21 CFR 864.9225 and under FDA product code KSP.

A type of device that is manufactured to send the chemicals and cells concurrently to the filter to obtain the cells in mass by filtering the cell only and passing the chemicals when extracting the cell for culturing for certain period by blending the chemical with the isotope and the cell.

Automated system for measurement of metabolic pathways, predominately glycolysis and mitochondrial respiration in real time assays

Replacment parts and accessories for automated cell metabolism analyzer systems

A pored mesh strainer that is inserted into a conical tube in order to rapidly remove debris or clots from a blood specimen and isolate primary cells in order to acquire a single cells suspension prior to flow cytometry or cell sorting analysis

Equipment that is designed to measure the flow from the properties of cement or concrete.

A tester for the stability of cement that is mixed and used on the mortar, and this tester examines the expandability, cracks, twisting and others.

A tester that is designed to measure the degree how much moisture can contain. For hydraulic cement, this is the tester that measures the moisture possession rate (%).

Crystal beads utilized during blood centrifugation to entrap fibrin and facilitate bioseparation of sample

In this classification a centrifugal chemistry analyzer for clinical use is an automatic device intended to centrifugally mix a sample and a reagent and spectrophotometrically measure concentrations of the sample constituents. This device is intended for use in conjunction with certain materials to measure a variety of analytes US FDA regulates Centrifugal chemistry analyzer for clinical use under 21 CFR 862.2140 and under FDA product code JJG.

A type of device that finds out the relationship with the radius in centrifugal force of object with the uniform circular motion and mass of object, period, and circular motion.

A microprocessor based circuit board that controls the operation, lid lock, speed and acceration or deceleration rate of a centrifuge

Attachment for centrifuge rotor that allows for the centrifugation of microplates

In this classification, this entry connotes a titrant of Ceric used as a reagent in clinical chemistry testing.

In this classification, a Ceruloplasmin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Ceruloplasmin. US FDA regulates Ceruloplasmin immunological test system under 21 CFR 866.5210 and under FDA product code DDB.

A tester that measures the chalking phenomenon that drops the pigment or paint powder when the dried surface is rubbed after painting or printing.

In this classification, this entry connotes an extract made of Cheese used in an Immunological Allergenic test.

A meter that measure the pollution in the water by using the chemical products heavy chrome acid potassium, potassium permanganate. When the organic matter, pollutant substance in water, is oxidized chemically, the organic matter is disintegrated in carbon gas and water to consume the oxygen, and the oxygen volume consumed is the value for chemical oxygen demand.

In this classification, this entry connotes an extract made of Chestnut used in an Immunological Allergenic test.

In this classification, Chlamydia serological reagents are devices used in test to identify specific Chlamydia antibodies in serum. US FDA regulates Chlamydia serological reagents under 21 CFR 866.3120 and under FDA product code GPW.

In this classification, this entry connotes a standardized formulation of Chlorate used to conduct Anion tests.

In this classification, this entry connotes a standardized formulation of Chloride used to conduct Anion tests.

In this classification, Chloride test system connotes a device used to measure Chloride levels. US FDA regulates Chloride test system under 21 CFR 862.1170 and under FDA product code JFS.

In this classification, this entry connotes a titrant of Chloride used as a reagent in clinical chemistry testing.

In this classification, this entry connotes a standardized formulation of Chlorine used to conduct Anion tests.

An instrument that measures excessiveness green pigment contained in the chloroplast of plants.

In this classification, this entry connotes a substrate made of Cholesterol that is used in clinical chemistry testing.

In this classification, Cholesterol (total) test system connotes a device used to measure Cholesterol (total) levels. US FDA regulates Cholesterol (total) test system under 21 CFR 862.1175 and under FDA product code NFX.

In this classification, this entry connotes a Cholinesterase enzyme that is used in clinical chemistry testing.

In this classification, a Cholinesterase test system is a device intended to measure Cholinesterase for clinical toxicology purposes. US FDA regulates Cholinesterase test system under 21 CFR 862.3240 and under FDA product code DLI

In this classification, Cholylglycine test system connotes a device used to measure Cholylglycine levels. US FDA regulates Cholylglycine test system under 21 CFR 862.1177 and under FDA product code KWW.

In this classification, this entry connotes a standardized formulation of Chromate used to conduct Anion tests.

In this classification a chromatographic separation material for clinical use is a device accessory intended for use in ion exchange chromatography, a procedure in which a compound is separated from a solution US FDA regulates Chromatographic separation material for clinical use under 21 CFR 862.2230 and under FDA product code DJY.

A blotting paper composed of superclean cotton or cellulose that is utilized during the stationary phase of thin layer chromatography to ensure wicking capability and uniformity of capillary action

Vial or insert or cap utilized for chromatographic bioanalytical autosampling and analysis

In this classification, a Chromogranin a tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Chromogranin a based tumors.

In this classification, a chromosome culture kit is a device containing the necessary ingredients (e.g., Minimum Essential Media (MEM) of McCoy's 5A culture media, phytohemagglutinin, fetal calf serum, antibiotics, and heparin) used to culture tissues for diagnosis of congenital chromosome abnormalities. US FDA regulates Chromosome culture kit under 21 CFR 864.2260 and under FDA product code KIQ.

In this classification, this entry connotes a Chymotrypsin enzyme that is used in clinical chemistry testing.

In this classification, Chymotrypsin test system connotes a device used to measure Chymotrypsin levels. US FDA regulates Chymotrypsin test system under 21 CFR 862.1180 and under FDA product code JKW.

A tester that is designed to measure the length of circumference or diameter of cigar or cigarette filter. It measures with the contact-type or noncontact-type, and there is device to measure the circumference and diameter simultaneously.

A meter that measures the air suction resistance of the finished and semi-finished filter products and measures the air suction resistance of cigarette. It measures the pressure difference when the air flow speed is set for 17.5mL/s.

Equipment that tests if the circuit breaker is appropriately functioned to switch the electric circuit under the abnormal condition for short-circuit breakdown and others.

A device for analyzing the molecular structure of an optically active substance by applying the electromagnetic field to linearly polarized light to generate left-handed and right-handed circularly polarized light and using the difference in molar extinction coefficient generated when circularly polarized light is passed through the sample.

In this classification, Citrobacter genus serological reagents are devices used in test to identify specific Citrobacter genus antibodies in serum. US FDA regulates Citrobacter genus serological reagents under 21 CFR 866.3125 and under FDA product code GTF.

A portable tester that is to measure the voltage, current, frequency, temperature, resistance and others of the line without peeling off the insulation material or cutting off the electric wire or circuit.

Certified apparel designed to operate in a cleanroom, maintaining an extremely low level of particulates (such as dust, airborne organisms, or vaporized particles) without contaminating the environment.

Certified footwear designed to operate in a cleanroom, maintaining an extremely low level of particulates (such as dust, airborne organisms, or vaporized particles) without contaminating the environment.

Specialty mats with adhesive substance that removes dirt and particles from bottom of shoes before entering cleanrooms or other environments to prevent contamination.

Chemistry analyzers can be benchtop devices or placed on a cart; other systems require floor space. They are used to determine the concentration of certain metabolites, electrolytes, proteins, and/or drugs in samples of serum, plasma, urine, cerebrospinal fluid, and/or other body fluids.

In this classification a clinical sample concentrator is a device intended to concentrate (by dialysis, evaporation, etc.) serum, urine, cerebrospinal fluid, and other body fluids before the fluids are analyzed US FDA regulates Clinical sample concentrator under 21 CFR 862.2310 and under FDA product code JJH.

In this classification, a Clinical toxicology calibrator is a device intended to measure Clinical toxicology calibratorfor clinical toxicology purposes. US FDA regulates Clinical toxicology calibrator under 21 CFR 862.3200 and under FDA product code DLJ

In this classification, a Clinical toxicology control material is a device intended to measure Clinical toxicology control material for clinical toxicology purposes. US FDA regulates Clinical toxicology control material under 21 CFR 862.3280 and under FDA product code DIF

In this classification, this entry connotes an extract made of Clover used in an Immunological Allergenic test.

A tube system comprised of microtubes that are attached in strips or blocks that are used for harvesting cells, cell uptake and receptor binding assays and/or radioimmunoassays

In this classification, a Coagulase plasma connotes a device used to create staphylothrombin, which enables the enzyme protease to convert fibrinogen, a plasma protein produced by the liver, to fibrin. This results in clotting of the blood. US FDA regulates Coagulase plasma under 21 CFR 866.2160 and under FDA product code JTL.

In this classification, a coagulation instrument is an automated or semi automated device used to determine the onset of clot formation for in vitro coagulation studies. US FDA regulates Coagulation instrument under 21 CFR 864.5400 and under FDA product code KQG.

In this classification, this entry connotes a standardized preparation made of Cobaltous chloride, used in a colorimetric Clinical laboratory test.

In this classification, a Cocaine and cocaine metabolite test system is a device intended to measure Cocaine and cocaine metabolite for clinical toxicology purposes. US FDA regulates Cocaine and cocaine metabolite test system under 21 CFR 862.3250 and under FDA product code DIO

In this classification, Coccidioides immitis serological reagents are devices used in test to identify specific Coccidioides immitis antibodies in serum. US FDA regulates Coccidioides immitis serological reagents under 21 CFR 866.3135 and under FDA product code GMH.

In this classification, this entry connotes an extract made of Cocklebur used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Cockroach used in an Immunological Allergenic test.

In this classification, a Codeine test system is a device intended to measure Codeine for clinical toxicology purposes. US FDA regulates Codeine test system under 21 CFR 862.3270 and under FDA product code LAD

In this classification, a Cohn fraction ii immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Cohn fraction ii. US FDA regulates Cohn fraction ii immunological test system under 21 CFR 866.5220 and under FDA product code DGA.

In this classification, a Cohn fraction iv immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Cohn fraction iv. US FDA regulates Cohn fraction iv immunological test system under 21 CFR 866.5360 and under FDA product code DAL.

In this classification, a Cohn fraction v immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Cohn fraction v. US FDA regulates Cohn fraction v immunological test system under 21 CFR 866.5370 and under FDA product code KHT.

Pre-operational automated engine test station designed to find and solve issues prior to running a hot test. Cold engine testing includes hooking up an engine or major component such as transmission, hydraulic cylinder, etc. to a dynamometer test station and cycling the engine component to pressure and flow check the component for defects or check for issues.

In this classification, this entry connotes a titrant of Collapse oxidation-reduction used as a reagent in clinical chemistry testing.

In this classification, a Colon cancer nat tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Colon cancer nat based tumors.

An instrument used to count colonies of bacteria or other microorganisms growing on an agar plate.

Color fastness means resistance of color on the dyeing substances based on the action influenced during the use or processing of dye thereof. This is a tester that is designed to test the color fastness.

In this classification a colorimeter, a photometer, or a spectrophotometer for clinical use is an instrument intended to measure radiant energy emitted, transmitted, absorbed, or reflected under controlled conditions. The device may include a monochromator to produce light of a specific wavelength US FDA regulates Colorimeter, photometer, or spectrophotometer for clinical use under 21 CFR 862.2300 and under FDA product code JJQ.

In this classification, a Colostrum immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Colostrum. US FDA regulates Colostrum immunological test system under 21 CFR 866.5230 and under FDA product code DGJ.

A tester that may comprehensively measure for voltage, current, frequency, wave form and others by consisting of power supplier, digital multi-meter, function generator, frequency counter and others.

Equipment that analyzes the combustion phenomenon of the substance in comprehensive term.

An instrument that is designed to measure the efficiency of an object that generates the light and heat by absorbing the surrounding oxygen. This is an instrument that measure the efficiency trough comparison with the calorie generated from the actual combustion process and the calorie generated from the complete combustion.

A tester that is designed to read automatically the abnormality of communication line for prompt inspection by simply determining the insulation condition between insulated conductor and insulated conductor and between insulated conductor and earth on the line of national boundaries and subscriber. Following the insulation resistance value of line, it is possible to determine with the visual discretion by the light-emitting diode lamp and hearing discretion by the warning sound, Also, it undertakes the test

In this classification, a Complement c2inhibitor (inactivator) immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Complement c2inhibitor (inactivator). US FDA regulates Complement c2inhibitor (inactivator) immunological test system under 21 CFR 866.5250 and under FDA product code DBA.

In this classification, a Complement c3binactivator immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Complement c3binactivator. US FDA regulates Complement c3binactivator immunological test system under 21 CFR 866.5260 and under FDA product code DAC.

In this classification, a Complement components immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Complement components. US FDA regulates Complement components immunological test system under 21 CFR 866.5240 and under FDA product code KTM.

In this classification, Complement reagent connotes a device that consists of complement, a naturally occurring serum protein from any warm-blooded animal such as guinea pigs, that may be included as a component part of serological test kits used in the diagnosis of disease. US FDA regulates Complement reagent under 21 CFR 866.4100 and under FDA product code KTQ.

In this classification, a Complexed prostatic specific antigen tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Complexed prostatic specific antigen based tumors.

A visual indicator of pressure that is set for 'zero' psi at atmospheric pressure and includes a dial which will continue to indicate the level of pressure above or below atmospheric pressure.

In this classification, Compound s (11-deoxycortisol) test system connotes a device used to measure Compound s (11-deoxycortisol) levels. US FDA regulates Compound s (11-deoxycortisol) test system under 21 CFR 862.1185 and under FDA product code JKB.

Machine that conducts compression resistance assays in bottles and packages, according to standard specifications.

A type of instrument that is designed to measure the volume of solute contained in the entire solution formed with the solvent and solute.

A testing instrument that measures the air volume contained in the concrete yet to be solidified.

A mold that is to form the cylinder specimen for testing the compression strength of the concrete.

A tester that measures the vibration of concrete used in road pavement or civil construction.

A type of device that measures the diameter of the specimen in conical-shaped cup made for the Korean Standard test table with the thin steel sheet from 0.5mm to 1.6mm.

In this classification, Conjugated sulfolithocholic acid (slcg) test system connotes a device used to measure Conjugated sulfolithocholic acid (slcg) levels. US FDA regulates Conjugated sulfolithocholic acid (slcg) test system under 21 CFR 862.1187 and under FDA product code KWX.

A tester that is used for the consolidation test that seeks the compression volume and compression speed when piling load, permitting the drainage toward the axis direction and restricting the soil surface.

A gridded or non gridded plate that containing a nutrient growth media that is used for monitoring necessary sanitary surfaces, by process of touching the agar to that surface for the growth, detection and enumeration of microorganisms that might be present there

A tester that measures the contact resistance generated when contacting with mutually different conductors.

In this classification a continuous flow sequential multiple chemistry analyzer for clinical use is a modular analytical instrument intended to simultaneously perform multiple chemical procedures using the principles of automated continuous flow systems. This device is intended for use in conjunction with certain materials to measure a variety of analytes US FDA regulates Continuous flow sequential multiple chemistry analyzer for clinical use under 21 CFR 862.2150 and under FDA product code JJC.

Equipment that is designed to test the capability and characteristic on several types of controller used for electric, electronic and communication.

Equipment that is designed to test the capability and characteristics of converter that is used for electric, electronic and communication circuit.

An industrial scale that consecutively measures the weight of properties that pass the above belt conveyor.

A type of device that is designed to measure the plane coordinates on the photo. It is the equipment that is the basis of interpretive photographic surveying e.g., aerotriangulation, application photographic surveying, cadastration, digital photogrammetry and others.

In this classification, this entry connotes a substrate made of Copper that is used in clinical chemistry testing.

In this classification, a copper sulfate solution for specific gravity determinations is a device used to determine whether the hemoglobin content of a potential donor's blood meets the required level (12.5 grams per 100 milliliters of blood for women and 13.5 grams per 100 milliliters of blood for men). US FDA regulates Copper sulfate solution for specific gravity determinations under 21 CFR 864.9320 and under FDA product code KSL.

In this classification, Copper test system connotes a device used to measure Copper levels. US FDA regulates Copper test system under 21 CFR 862.1190 and under FDA product code JKZ.

In this classification, this entry connotes an extract made of Corn used in an Immunological Allergenic test.

In this classification, Corticoids test system connotes a device used to measure Corticoids levels. US FDA regulates Corticoids test system under 21 CFR 862.1195 and under FDA product code CHE.

In this classification, Corticosterone test system connotes a device used to measure Corticosterone levels. US FDA regulates Corticosterone test system under 21 CFR 862.1200 and under FDA product code CHA.

In this classification, Cortisol (hydrocortisone and hydroxycorticosterone) test system connotes a device used to measure Cortisol (hydrocortisone and hydroxycorticosterone) levels. US FDA regulates Cortisol (hydrocortisone and hydroxycorticosterone) test system under 21 CFR 862.1205 and under FDA product code NHG.

In this classification, Corynebacterium genus serological reagents are devices used in test to identify specific Corynebacterium genus antibodies in serum. US FDA regulates Corynebacterium genus serological reagents under 21 CFR 866.3140 and under FDA product code KFI.

In this classification, this entry connotes an extract made of Cottonwood used in an Immunological Allergenic test.

In this classification, Coxsackievirus serological reagents are devices used in test to identify specific Coxsackievirus antibodies in serum. US FDA regulates Coxsackievirus serological reagents under 21 CFR 866.3145 and under FDA product code GNG.

In this classification, C-peptides of proinsulin test system connotes a device used to measure C-peptides of proinsulin levels. US FDA regulates C-peptides of proinsulin test system under 21 CFR 862.1135 and under FDA product code JKD.

A scale that measures the object with the scale attached on the ceiling to measure the weight. The display part is digitalized and widely used in the construction sites and industrial settings.

In this classification, a C-reactive protein immunological test system is a device that consists of the reagents used to identify by immunochemical techniques C-reactive protein. US FDA regulates C-reactive protein immunological test system under 21 CFR 866.5270 and under FDA product code DCN.

In this classification, this entry connotes a Creatine kinase enzyme that is used in clinical chemistry testing.

In this classification, this entry connotes a Creatine kinase - mb enzyme that is used in clinical chemistry testing.

In this classification, Creatine phosphokinase/creatine kinase or isoenzymes test system connotes a device used to measure Creatine phosphokinase/creatine kinase or isoenzymes levels. US FDA regulates Creatine phosphokinase/creatine kinase or isoenzymes test system under 21 CFR 862.1215 and under FDA product code JHS.

In this classification, Creatine test system connotes a device used to measure Creatine levels. US FDA regulates Creatine test system under 21 CFR 862.1210 and under FDA product code JLA.

In this classification, this entry connotes a substrate made of Creatinine that is used in clinical chemistry testing.

In this classification, Creatinine test system connotes a device used to measure Creatinine levels. US FDA regulates Creatinine test system under 21 CFR 862.1225 and under FDA product code JFY.

Cryogenic storage system for bacteria that is composed of a cryovial incorporating treated beads and special cryopreservative solution

Flexible bio-compatible cylinder for storage of materials for assisted reproduction. Tube ends are crimped to contain specimen.

Bag and protective overwrap used for long term cryogenic freezing, storage and thawing of human blood components and cells

Stepped metal cane used for long term vial and tube cryogenic storage

Label and writing marker used for cryogenic specimen identification that are specially formulated to withstand ultra low freezing temperatures

Plasma derived concentrate of fibrogen, fibronectin and clotting factors.

In this classification, Cryptococcus neoformans serological reagents are devices used in test to identify specific Cryptococcus neoformans antibodies in serum. US FDA regulates Cryptococcus neoformans serological reagents under 21 CFR 866.3165 and under FDA product code GME.

A tester that is designed to measure and test the crystal factor of resonance frequency, impedance and others if the frequency control function is appropriate at the designated frequency for crystal resonator used in frequency control in wireless transmitter and others.

In this classification, cultured animal and human cells are in vitro cultivated cell lines from the tissue of humans or other animals which are used in various diagnostic procedures, particularly diagnostic virology and cytogenetic studies. US FDA regulates Cultured animal and human cells under 21 CFR 864.2280 and under FDA product code KIR.

In this classification a culture medium for antimicrobial susceptibility tests is a device intended for medical purposes that consists of any medium capable of supporting the growth of many of the bacterial pathogens that are subject to antimicrobial susceptibility tests. The medium should be free of components known to be antagonistic to the common agents for which susceptibility tests are performed in the treatment of disease US FDA regulates Culture medium for antimicrobial susceptibility tests under 21 CFR 866.1700 and under FDA product code LKA.

In this classification, a Culture medium for pathogenicneisseria spp. connotes a device used for culturing and primarily isolating pathogenic Neisseria bacteria, including Neisseria gonorrhoeae and Neisseria meningitidis US FDA regulates Culture medium for pathogenicneisseria spp. under 21 CFR 866.2410 and under FDA product code JTY.

All viral and microbial culture collection and transport containers without swabs

In this classification, this entry connotes a standardized preparation made of Cupric sulfate, used in a colorimetric Clinical laboratory test.

A shunt resistor that uses the meter in parallel to flow certain ratio of the measured current to measure the current in excess to the maximum scale figure of ammeter.

Device to test the amount of electrical energy flowing through an electrical line.

A meter that is design to measure the flowing speed of the fluid. There are the impeller type and the pitot tube-type.

A device that converts the input signal of current into an output signal of another form.

Test equipment that tests the potential transformer and current transformer. It tests the highest voltage, insulation level, rated current, rated voltage, rated frequency and others.

A type of instrument designed for measuring the length of curved and crooked lines plotted on topographic plans, maps and graphical documents.

An instrument that is designed to measure the size of cutting resistance under the base study for the tool geometry or cutting process. Cutting force is the resistance force received by the tool when the workpiece is processed for cutting.

In this classification, this entry connotes a standardized formulation of Cyanide used to conduct Anion tests.

In this classification, Cyclic amp test system connotes a device used to measure Cyclic amp levels. US FDA regulates Cyclic amp test system under 21 CFR 862.1230 and under FDA product code CHO.

In this classification, Cyclosporine test system connotes a device used to measure Cyclosporine levels. US FDA regulates Cyclosporine test system under 21 CFR 862.1235 and under FDA product code MKW.

In this classification, a Cyfra 21-1 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Cyfra 21-1 based tumors.

Equipment that is used to measure the diameter of conical-shaped products that may easily cause deformation on the size or get dirty when contacted or when it is in the condition of easily fragile, elasticity or high temperature.

A precision tool that is structured with the character board indicator installed on the pulley that moves on the support frame.

In this classification, this entry connotes an extract made of Cypress used in an Immunological Allergenic test.

In this classification, a Cystic fibrosis transmembrane conductance regulator (cftr) gene mutation detection system is a device that consists of the reagents used to identify by immunochemical techniques Cystic fibrosis transmembrane conductance regulator (cftr) gene mutation detection. US FDA regulates Cystic fibrosis transmembrane conductance regulator (cftr) gene mutation detection system under 21 CFR 866.5900 and under FDA product code PFS.

In this classification, Cystine test system connotes a device used to measure Cystine levels. US FDA regulates Cystine test system under 21 CFR 862.1240 and under FDA product code JLD.

In this classification a Cytocentrifuge connotes a device that is a low-speed, low-acceleration centrifuge used to separate cellular material without damaging it US FDA regulates Cytocentrifuge under 21 CFR 864.3300 and under FDA product code IFB.

Funnel, filter card and/or clamping device utilized on a cytocentrifuge for sample concentration to perform cytological, hematological or histological examination

Liquid based processing system for gynecological and non gynecological specimens in which the specimen is drawn through a processor for the removal of debris and then is deposited as a thin cell preparation on a microscope slide for staining and examination

In this classification, Cytomegalovirus serological reagents are devices used in test to identify specific Cytomegalovirus antibodies in serum. US FDA regulates Cytomegalovirus serological reagents under 21 CFR 866.3175 and under FDA product code GQH.

In this classification, this entry connotes an extract made of Daisy used in an Immunological Allergenic test.

Programmable recording system utlized for sampling, recording and storage of all temperature data for clinical equipment and instruments such as freezers, refrigerators, incubators, storage containers, controlled transport and other application with critical temperature requirements

dB Meter is full of features sound level meter with exclusive accuracy of measurements plus Hearing test, Noise dosimeter, Spectrum Analyzer with RTA, FFT & Spectrogram.

In this classification, Dehydroepiandrosterone (free and sulfate) test system connotes a device used to measure Dehydroepiandrosterone (free and sulfate) levels. US FDA regulates Dehydroepiandrosterone (free and sulfate) test system under 21 CFR 862.1245 and under FDA product code JKC.

In this classification, this entry connotes a substrate made of Delta-aminolaevulinic acid that is used in clinical chemistry testing.

In this classification, Delta-aminolevulinic acid test system connotes a device used to measure Delta-aminolevulinic acid levels. US FDA regulates Delta-aminolevulinic acid test system under 21 CFR 862.1060 and under FDA product code JKL.

A tester that measures the demulsibility, a property to separate into the individual substance for emulsion.

A meter that is designed to measure the height of building structure, tree or others.

In this classification a densitometer/scanner (integrating, reflectance, thin-layer chromatography, or radio chromatogram) for clinical use is device intended to measure the concentration of a substance on the surface of a film or other support media by either a photocell measurement of the light transmission through a given area of the medium or, in the case of the radio chromatogram scanner, by measurement of the distribution of a specific radio-active element on a radio chromatogram US FDA regulates Densitometer/scanner (integrating, reflectance, tlc, or radio chromatogram) for clinical use under 21 CFR 862.2400 and under FDA product code JQT.

A type of instrument that measures density --volume for each unit-- that is the basic properties of a substance.

Equipment that disposes in mass of manifestation for genes, search for genetic disease, virus infection and others.

It is a laboratory instrument with accessories used to keep a substance clean and dehydrated through vacuum

In this classification, Desoxycorticosterone test system connotes a device used to measure Desoxycorticosterone levels. US FDA regulates Desoxycorticosterone test system under 21 CFR 862.1250 and under FDA product code JLE.

In this classification, a device for sealing microsections is an automated instrument used to seal stained cells and microsections for histological and cytological examination. US FDA regulates Device for sealing microsections under 21 CFR 864.34 and under FDA product code KIM.

An instrument that is to measure the dew point temperature at the atmosphere. It is the thermometer that measures the temperature when there is any dew or frost by gradual cooling down of the metal surface.

A type of instrument used to accurately measure a small distance. Also known as a Dial gauge or Dial Test Indicator (DTI)

Slide cassettes for low molecular weight exchange, concentration and desalting

Device used to hold dialysis slide cassettes

Flask used in laboratory dialysis for the removal of buffer salts and small contaminants from proteins and other macromolecules in sample volumes up to 250 mL

Membranes utilized in dialysis cassettes for low molecular weight exchange, concentration and desalting

In this classification, this entry connotes a titrant of Dichromate used as a reagent in clinical chemistry testing.

A type of device that analyzes the quantity with the dietary fiber ingredients contained in the food and others.

In this classification, a Differential culture medium connotes a device used that consists primarily of liquid or solid biological materials intended for medical purposes for the cultivation and identification of particular organisms.  US FDA regulates Differential culture medium under 21 CFR 866.2320 and under FDA product code JSH.

A measurement instrument designed to measure the difference between two pressure sources.

In this classification, a Digitoxin test system is a device intended to measure Digitoxin for clinical toxicology purposes. US FDA regulates Digitoxin test system under 21 CFR 862.3300 and under FDA product code DKQ

In this classification, a Digoxin test system is a device intended to measure Digoxin for clinical toxicology purposes. US FDA regulates Digoxin test system under 21 CFR 862.3320 and under FDA product code DKA

In this classification, a Diphenylhydantoin test system is a device intended to measure Diphenylhydantoin for clinical toxicology purposes. US FDA regulates Diphenylhydantoin test system under 21 CFR 862.3350 and under FDA product code DIP

In this classification a discrete photometric chemistry analyzer for clinical use is a device intended to duplicate manual analytical procedures by performing automatically various steps such as pipetting, preparing filtrates, heating, and measuring color intensity. This device is intended for use in conjunction with certain materials to measure a variety of analytes US FDA regulates Discrete photometric chemistry analyzer for clinical use under 21 CFR 862.2160 and under FDA product code JJE.

A tester that evaluates and tests the dispersion, cohesion, and safety of disperse system like colloid.

An instrument that measures by converting the displacement into the electric volume and others.

A transducer that physically moves in response to a change in condition. Displacement transducers are often used for precision measurement of small distances where traditional contact methods of measurement are not feasible

Displacement instruments determine liquid level by sensing the buoyant force exerted on a displacer by the liquid it displaces. Unlike floats, in float‐type level instruments, the displacer moves very little relative to the rising or falling liquid.

An analyzer that promptly analyzes several ingredients melted in the solution simultaneously.

Both distilled and deionized water is water that has been purified. Distilled water is water that has had all its impurities removed by boiling. Deionized water is water that lacks ions, causing the waters resistivity to increase. It is similar to distilled water and is useful for scientific experiments. It also can be used for a short time as a high voltage dielectric in some pulsed power applications.

A meter that read the degree of distortion of the signal. The series resonance bridge or Wien bridge is generally used to remove the fundamental wave, and the remaining harmonics and noise ingredient are compared and measured with the fundamental wave and this would measure the degree of noise.

In this classification, this entry connotes an extract made of Dock used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Dogwood used in an Immunological Allergenic test.

A device used for measuring the weight of a piece of personal baggage. The weight is usually measured by suspending the luggage beneath the scale secured by a hook or a strap

Donor unit tubing piercing sampler that dispenses donor blood for crossmatch immunohematology

A type of device that measures the pressure difference on the front and back of the wing wheel to know the air flow in the fan or ventilator.

A type of standard gauge that is made with each step for the size sequence. It is used to measure the diameters of drill, tap, machine screw, and general wire rod.

A tester that is designed to measure appropriate temperature as the lowest temperature that begins to drop in liquid phase for a part thereof when the semi-solid substances (grease, wax and others) are heated.

A tester that is designed to test the impact resistance of the packing material, impact resistance of contents in the package, appropriateness of packing material, strength comparison of packing box, impact resistance strength of actual goods by dropping packed cargo, packing box or small device from certain height.

In this classification, a Drug metabolizing enzyme genotyping system is a device intended to measure Drug metabolizing enzyme genotypesfor clinical toxicology purposes. US FDA regulates Drug metabolizing enzyme genotyping system under 21 CFR 862.3360 and under FDA product code NTI

A glass device that is to remove the moisture contained in various gases and vapor samples.

In this classification, this entry connotes an extract made of Dust used in an Immunological Allergenic test.

In this classification, this entry connotes a substrate made of D-xylose that is used in clinical chemistry testing.

In this classification, a Early prostate cancer antigen - 2 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Early prostate cancer antigen - 2 based tumors.

An instrument for tool measurement that is used to measure eccentricity of several tools, arbor, shaft and saw tooth, and used for the measurement of circular shapes.

In this classification, Echinococcus genus serological reagents are devices used in test to identify specific Echinococcus genus antibodies in serum. US FDA regulates Echinococcus genus serological reagents under 21 CFR 866.3200 and under FDA product code GPF.

Instrument for acoustic detection

In this classification, Echovirus serological reagents are devices used in test to identify specific Echovirus antibodies in serum. US FDA regulates Echovirus serological reagents under 21 CFR 866.3205 and under FDA product code GNL.

In this classification, this entry connotes a reagent made of Edta disodium aqueous solution used in clinical chemistry testing.

In this classification, this entry connotes a standardized formulation of Edta used to conduct Anion tests.

In this classification, this entry connotes a titrant of Edta used as a reagent in clinical chemistry testing.

In this classification, this entry connotes an extract made of Egg used in an Immunological Allergenic test.

A clip that is designed to promptly and temporarily connect the electric signal.

A micrometer that is indicated by amplifying electrically and converting the finite displacement volume of measuring ruler for contact type into quantity of electricity.

A tester that indicates if the electric power has stable strength and frequency for the electric power generation, conversion and transmission and distribution system.

A device that converts one form of electrical energy into another form of electrical energy.

Equipment that is used for the maintenance and repairing on the electric rail car. This is exclusive tester for electric rail car that confirms and inspects the motion condition and capability of various parts.

Automated system utilized for sodium, potassium, chloride, carbon dioxide and lithium quantitation

Reagents for use with the electrolyte analyzer for testing electrolytes such as Na, K, CL.

A tester that tests whether the electric energy generated by radiation, conduction, radio frequency interference and others from electricity, electronic, and information devices through the public air and connected circuit and line would not provide adverse effect of electric energy to the human body and whether it would meet the standard value permitted not to generate the interference, such as erroneous motion, functional decline, damage and others of other devices.

An electromagnetic shielded room that is designed to test the appropriateness on electromagnetic interference of electric, electronic, and information device.

A type of device that is designed to test the susceptibility on the external electromagnetic wave of electric, electronic and information device not to be interferes for erroneous motion, function decline, damage and others with respect to the electromagnetic wave having the electric and magnetic energy, such as static electricity, voltage, frequency and others that may be received from the outside for electric, electronic and information device.

A meter that is designed to measure the ratio with the phase velocity of wave in free space and the phase velocity of wave in the given medium space.

A digital weighing scale is the most accurate and precise analog front-end (AFE) instrument that uses force sensors to measure the load of an object.

A device used to detect electrons and X-ray which are generated when the electronic gun shoots an electronic beam and conduct quantitative and qualitative analysis on the elements.

Equipment that is designed to analyze the characteristics of the sample surface by measuring the binding energy of the photoelectron discharged by the light.

A meter that is used to clarify the micro-structure of distribution of impure substance within the sample, lattice defect or others by measuring the influence of the internal magnetic field by the neighboring electron or atomic nucleus spin when there is any electron not paired within the sample.

In this classification an electrophoresis apparatus for clinical use is a device intended to separate molecules or particles, including plasma proteins, lipoproteins, enzymes, and hemoglobulins on the basis of their net charge in specified buffered media. This device is used in conjunction with certain materials to measure a variety of analytes as an aid in the diagnosis and treatment of certain disorders US FDA regulates Electrophoresis apparatus for clinical use under 21 CFR 862.2485 and under FDA product code JJN.

Applicator and blade utilized to apply samples to an electrophoretic film

A type of device that moves the molecules with the electric features within the electric field. It is frequently used for the measurement of molecule volume in substance and separation of substance used of the difference for quantity of electricity or forms of each substance.

In this classification an electrophoretic hemoglobin analysis system is a device that electrophoretically separates and identifies normal and abnormal hemoglobin types as an aid in the diagnosis of anemia or erythrocytosis (increased total red cell mass) due to a hemoglobin abnormality US FDA regulates Electrophoretic hemoglobin analysis system under 21 CFR 864.7440 and under FDA product code OOX.

Cuvette, plate, or chamber based system utilized for inserting or transfection of molecules into mammalian cells by using an electrical pulse to create pores in the cell membrane through which those molecules can pass

A type of device that analyzes the ingredient elements that structure the organic compounds.

Equipment that analyzes the structure of the thin film by measuring the thin film thickness, refraction rate, extinction coefficient, and density with the change shown when reflecting the laser or polarized light on the sample.

In this classification, this entry connotes an extract made of Elm used in an Immunological Allergenic test.

In this classification, An empty container for the collection and processing of blood and blood components is a device intended for medical purposes that is an empty plastic bag or plastic or glass bottle used to collect, store, or transfer blood and blood components for further processing. US FDA regulates Empty container for the collection and processing of blood and blood components under 21 CFR 864.9100 and under FDA product code KSR.

In this classification, Endotoxin assay are devices used in test to identify specific Endotoxin assay antibodies in serum. US FDA regulates Endotoxin assay under 21 CFR 866.3210 and under FDA product code NGS.

In this classification, a Enriched culture medium connotes a device used that consists primarily of specific and known qualities that favors the growth of a particular microorganism. US FDA regulates Enriched culture medium under 21 CFR 866.2330 and under FDA product code KZI.

In this classification, Entamoeba histolytica serological reagents are devices used in test to identify specific Entamoeba histolytica antibodies in serum. US FDA regulates Entamoeba histolytica serological reagents under 21 CFR 866.3220 and under FDA product code KHW.

In this classification, Enterovirus nucleic acid assay are devices used in test to identify specific Enterovirus nucleic acid assay antibodies in serum. US FDA regulates Enterovirus nucleic acid assay under 21 CFR 866.3225 and under FDA product code OAI.

In this classification, an environmental chamber for storage of platelet concentrate is a device used to hold platelet-rich plasma within a preselected temperature range. US FDA regulates Environmental chamber for storage of platelet concentrate under 21 CFR 864.9575 and under FDA product code KSH.

In this classification an enzyme analyzer for clinical use is a device intended to measure enzymes in plasma or serum by nonkinetic or kinetic measurement of enzyme-catalyzed reactions. This device is used in conjunction with certain materials to measure a variety of enzymes as an aid in the diagnosis and treatment of certain enzyme-related disorders US FDA regulates Enzyme analyzer for clinical use under 21 CFR 862.2500 and under FDA product code JJI.

This commodity includes disposable plastic laboratory supplies for enzyme and protein expression that are treated or coated (organic or inorganic) to improve performance.

A test kit that uses antibodies and color change to identify a substance

In this classification Enzyme preparations are products that are used in the histopathology laboratory for the following purposes: to disaggregate tissues and cells already in established cultures for preparation into subsequent cultures (e.g., trypsin); to disaggregate fluid specimens for cytological examination (e.g., papain for gastric lavage or trypsin for sputum liquefaction); to aid in the selective staining of tissue specimens (e.g., diastase for glycogen determination). US FDA regulates Enzyme preparations under 21 CFR 864.4400 and under FDA product code IBC.

In this classification, this entry connotes a colorimetric standard that incorporates the Ep Color Index.

In this classification, Epstein-barr virus serological reagents are devices used in test to identify specific Epstein-barr virus antibodies in serum. US FDA regulates Epstein-barr virus serological reagents under 21 CFR 866.3235 and under FDA product code GNP.

In this classification, Equine encephalomyelitis virus serological reagents are devices used in test to identify specific Equine encephalomyelitis virus antibodies in serum. US FDA regulates Equine encephalomyelitis virus serological reagents under 21 CFR 866.3240 and under FDA product code GQD.

A tester that measures the Erichsen value that displays the degree of plastic deformation that flattens the metal well.

In this classification, Erysipelothrix rhusiopathiae serological reagents are devices used in test to identify specific Erysipelothrix rhusiopathiae antibodies in serum. US FDA regulates Erysipelothrix rhusiopathiae serological reagents under 21 CFR 866.3250 and under FDA product code GSD.

In this classification, Erythrocyte sedimentation rate test connotes a device used to measure the length of time required for the red cells in a blood sample to fall a specified distance or a device that measures the degree of sedimentation taking place in a given length of time. An increased rate indicates tissue damage or inflammation. US FDA regulates Erythrocyte sedimentation rate test under 21 CFR 864.6700 and under FDA product code JPH.

In this classification an erythrocytic glucose-6-phosphate dehydrogenase assay is a device used to measure the activity of the enzyme glucose-6-phosphate dehydrogenase or of glucose-6-phosphate dehydrogenase isoenzymes. The results of this assay are used in the diagnosis and treatment of nonspherocytic congenital hemolytic anemia or drug-induced hemolytic anemia associated with a glucose-6-phosphate dehydrogenase deficiency. This generic device includes assays based on fluorescence, electrophoresis, methemoglobin reduction, catalase inhibition, and ultraviolet kinetics US FDA regulates Erythrocytic glucose-6-phosphate dehydrogenase assay under 21 CFR 864.736 and under FDA product code JBI.

In this classification a erythropoietin assay is a device that measures the concentration of erythropoietin (an enzyme that regulates the production of red blood cells) in serum or urine. This assay provides diagnostic information for the evaluation of erythrocytosis (increased total red cell mass) and anemia US FDA regulates Erythropoietin assay under 21 CFR 864.7250 and under FDA product code GGT.

In this classification, Escherichia coli serological reagents are devices used in test to identify specific Escherichia coli antibodies in serum. US FDA regulates Escherichia coli serological reagents under 21 CFR 866.3255 and under FDA product code GMZ.

In this classification, Estradiol test system connotes a device used to measure Estradiol levels. US FDA regulates Estradiol test system under 21 CFR 862.1260 and under FDA product code CHP.

In this classification, Estriol test system connotes a device used to measure Estriol levels. US FDA regulates Estriol test system under 21 CFR 862.1265 and under FDA product code CGI.

In this classification, a Estrogen receptor assays tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Estrogen receptor assays based tumors.

In this classification, Estrogens (total, in pregnancy) test system connotes a device used to measure Estrogens (total, in pregnancy) levels. US FDA regulates Estrogens (total, in pregnancy) test system under 21 CFR 862.1270 and under FDA product code CHM.

In this classification, Estrogens (total, nonpregnancy) test system connotes a device used to measure Estrogens (total, nonpregnancy) levels. US FDA regulates Estrogens (total, nonpregnancy) test system under 21 CFR 862.1275 and under FDA product code JMD.

In this classification, Estrone test system connotes a device used to measure Estrone levels. US FDA regulates Estrone test system under 21 CFR 862.1280 and under FDA product code CGF.

In this classification, a Ethosuximide test system is a device intended to measure Ethosuximide for clinical toxicology purposes. US FDA regulates Ethosuximide test system under 21 CFR 862.3380 and under FDA product code DLF

In this classification, Etiocholanolone test system connotes a device used to measure Etiocholanolone levels. US FDA regulates Etiocholanolone test system under 21 CFR 862.1285 and under FDA product code JLF.

In this classification a euglobulin lysis time test is a device that measures the length of time required for the lysis (dissolution) of a clot formed from fibrinogen in the euglobulin fraction (that fraction of the plasma responsible for the formation of plasmin, a clot lysing enzyme) US FDA regulates Euglobulin lysis time tests under 21 CFR 864.7275 and under FDA product code JBO.

A space that the facilities are equipped to make the explosives in order to measure the impact on animals and plants, service life and other characteristics of various machines and equipments with the explosion.

An instrument that is to measure the volume of the surface water attached on the aggregate surface by using the chemical reaction of carbide powder and water in the closed container.

In this classification a factor deficiency test is a device used to diagnose specific coagulation defects, to monitor certain types of therapy, to detect coagulation inhibitors, and to detect a carrier state (a person carrying both a recessive gene for a coagulation factor deficiency such as hemophilia and the corresponding normal gene) US FDA regulates Factor deficiency test under 21 CFR 864.7290and under FDA product code GGP.

In this classification Factor V Leiden deoxyribonucleic acid (DNA) mutation detection systems are devices that consist of different reagents and instruments which include polymerase chain reaction (PCR) primers, hybridization matrices, thermal cyclers, imagers, and software packages US FDA regulates Factor v leiden dna mutation detection systems under 21 CFR 864.7280 and under FDA product code NPQ.

In this classification, a Factor xiii, a, s, immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Factor xiii, a, s,. US FDA regulates Factor xiii, a, s, immunological test system under 21 CFR 866.5330 and under FDA product code DBT.

Fast optical 96 well reaction plate reduces PCR reaction time from 2 hours to as little as 25 minutes.

A device used in Fast Protein Liquid Chromatography FPLC systems.

A type of column chromatography system used to separate or purify proteins from complex mixtures.It is very commonly used in biochemistry and enzymology.

In this classification, Fatty acids test system connotes a device used to measure Fatty acids levels. US FDA regulates Fatty acids test system under 21 CFR 862.1290 and under FDA product code JLH.

In this classification, a Fecal calprotectin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Fecal calprotectin. US FDA regulates Fecal calprotectin immunological test system under 21 CFR 866.5180 and under FDA product code NXO.

In this classification, this entry connotes a standardized preparation made of Ferric chloride, used in a colorimetric Clinical laboratory test.

In this classification, a Ferritin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Ferritin. US FDA regulates Ferritin immunological test system under 21 CFR 866.5340 and under FDA product code DBF.

In this classification, this entry connotes a titrant of Ferrous ammonium sulfate used as a reagent in clinical chemistry testing.

In this classification, this entry connotes an extract made of Fescue used in an Immunological Allergenic test.

In this classification a fetal hemoglobin assay is a device that is used to determine the presence and distribution of fetal hemoglobin (hemoglobin F) in red cells or to measure the amount of fetal hemoglobin present. The assay may be used to detect fetal red cells in the maternal circulation or to detect the elevated levels of fetal hemoglobin exhibited in cases of hemoglobin abnormalities such as thalassemia (a hereditary hemolytic anemia characterized by a decreased synthesis of one or more types of hemoglobin polypeptide chains). The hemoglobin determination may be made by methods such as electrophoresis, alkali denaturation, column chromatography, or radial immunodiffusion US FDA regulates Fetal hemoglobin assay under 21 CFR 864.7455 and under FDA product code KQI.

A tester that measures the length of fiber, the most important feature for various fibers.

In this classification a fibrin monomer paracoagulation test is a device used to detect fibrin monomer in the diagnosis of disseminated intravascular coagulation (non localized clotting within a blood vessel) or in the differential diagnosis between disseminated intravascular coagulation and primary fibrinolysis (dissolution of the fibrin in a blood clot) US FDA regulates Fibrin monomer Para coagulation test under 21 CFR 864.7300 and under FDA product code JBM.

In this classification a fibrinogen determination system is a device that consists of the instruments, reagents, standards, and controls used to determine the fibrinogen levels in disseminated intravascular coagulation (non localized clotting within the blood vessels) and primary fibrinolysis (the dissolution of fibrin in a blood clot) US FDA regulates Fibrinogen determination system under 21 CFR 864.734 and under FDA product code KQJ.

In this classification a fibrinogen/fibrin degradation products assay is a device used to detect and measure fibrinogen degradation products and fibrin degradation products (protein fragments produced by the enzymatic action of plasmin on fibrinogen and fibrin) as an aid in detecting the presence and degree of intravascular coagulation and fibrinolysis (the dissolution of the fibrin in a blood clot) and in monitoring therapy for disseminated intravascular coagulation (non localized clotting in the blood vessels) US FDA regulates Fibrinogen/fibrin degradation products assay under 21 CFR 864.7320 and under FDA product code MIF.

In this classification, a Fibrinopeptide a immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Fibrinopeptide a. US FDA regulates Fibrinopeptide a immunological test system under 21 CFR 866.5350 and under FDA product code DAN.

A type of device that is used for sample preparation to test the film capability of paint.

In this classification, this entry connotes an extract made of Fir used in an Immunological Allergenic test.

A tester that measures the igniting temperature that means the combustibles would be required to reach certain temperature from the outside heat to make itself burning.

A flow meter which is installed to confirm the amount of rated flux by undertaking the operation and capability tests for rated load of fire extinguishing pump at the time of installing the pump and regular inspection.

In this classification, this entry connotes an extract made of Fireweed used in an Immunological Allergenic test.

In this classification a flame emission photometer for clinical use is a device intended to measure the concentration of sodium, potassium, lithium, and other metal ions in body fluids. Abnormal variations in the concentration of these substances in the body are indicative of certain disorders (e.g., electrolyte imbalance and heavy metal intoxication) and are, therefore, useful in diagnosis and treatment of those disorders US FDA regulates Flame emission photometer for clinical use under 21 CFR 862.2540 and under FDA product code JJO.

A material that is used in the reaction experiment of the oxidizing flame.

Automated system for the quantitation of sodium, potassium, chloride and lithium in serum, plasma or aqueous solutions, utilizing spectral ray measurement following sample vaporization by an extremely hot flame

Replacement parts and accessories utilitzed for automated flame photometric analyzer systems

Reagent or kit utilized for the quantitation of sodium, potassium, chloride and lithium in serum, plasma or aqueous solutions by automated flame photometric analysis

Flammability indicates the degree of resistance to the flame for certain material. It is stringently regulated for clothes, interior materials, construction materials and others, and there are several types of tester in accordance with the product use and test method.

Weight or weighted ring placed on the neck of a flask to stabilize it in water baths or applications that place the flask at risk for toppling

In this classification, Flavobacterium genus serological reagents are devices used in test to identify specific Flavobacterium genus antibodies in serum. US FDA regulates Flavobacterium genus serological reagents under 21 CFR 866.3270 and under FDA product code GSW.

Equipment that measures the weight center of the gravity in floating body including stability, neutral, unstable and others for the object floating on the liquid surface. Floating pontoon is launched on the water tank to measure the center of floating body, and it measures the change of metacenter height following the slope of the metacenter and the floating body from metacenter height to experiment the stability of the floating body.

A device that makes the quality and quantity analysis on sell particle size, internal structure and others of sample by measuring the scattered light and fluorescence radiated by individual particle with the irradiation of excitation light on the thin current flowing down the particles, such as dyed cell with fluorescence and others.

Replacement parts, accessories and supplies for flow cytometric analysis

Automated system for laser based cell counting and sorting, biomarker monitoring and other biophysical applications by suspension in fluid and passage through a detection system

All quality controls, calibrator beads, and standards utilized in flow cytometric analysis

A device that detects the presence of finite defect existing on the surface of the material by using the fluorescent solution. It is used for the flaw test of casting material, forging material, rolling material, welding material and others.

In this classification, this entry connotes a standardized formulation of Fluoride used to conduct Anion tests.

In this classification a fluorometer for clinical use is a device intended to measure by fluorescence certain analytes. Fluorescence is the property of certain substances of radiating, when illuminated, a light of a different wavelength. This device is used in conjunction with certain materials to measure a variety of analytes US FDA regulates Fluorometer for clinical use under 21 CFR 862.2560 and under FDA product code KHO.

In this classification, Folic acid test system connotes a device used to measure Folic acid levels. US FDA regulates Folic acid test system under 21 CFR 862.1295 and under FDA product code CGN.

In this classification, Follicle-stimulating hormone test system connotes a device used to measure Follicle-stimulating hormone levels. US FDA regulates Follicle-stimulating hormone test system under 21 CFR 862.1300 and under FDA product code NGA.

In this classification, this entry connotes an extract made of Food used in an Immunological Allergenic test.

In this classification, this entry connotes a standardized formulation of Formate used to conduct Anion tests.

In this classification, Formiminoglutamic acid (figlu) test system connotes a device used to measure Formiminoglutamic acid (figlu) levels. US FDA regulates Formiminoglutamic acid (figlu) test system under 21 CFR 862.1305 and under FDA product code JLI.

A type of fraction collector used to separate liquid according to density which is parted from columns such as liquid chromatography, and automatically form a liquid layer within the centrifugal separating tube.

In this classification, Francisella tularensis serological reagents are devices used in test to identify specific Francisella tularensis antibodies in serum. US FDA regulates Francisella tularensis serological reagents under 21 CFR 866.3280 and under FDA product code GSL.

In this classification, a Free prostatic specific antigen tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Free prostatic specific antigen based tumors.

In this classification, a Free secretory component immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Free secretory component. US FDA regulates Free secretory component immunological test system under 21 CFR 866.5380 and under FDA product code DAJ.

In this classification, Free thyroxine test system connotes a device used to measure Free thyroxine levels. US FDA regulates Free thyroxine test system under 21 CFR 862.1695 and under FDA product code CEC.

In this classification, Free tyrosine test system connotes a device used to measure Free tyrosine levels. US FDA regulates Free tyrosine test system under 21 CFR 862.1730 and under FDA product code CRD.

A type of tester that tests the resistance on freezing and thawing of liquid phase or mortar.

An instrument that is used to measure the freezing point and estimate the molecular weight of the substance.

For measurements of frequency, time interval, phase, event counting, and many other related signal parameters

A type of device that tests the equipment that controls the frequency to be available for any narrow range from the power plant.

A meter that measures the maximum value of difference of instantaneous frequency of modulated wave and carrier frequency --non-modulation frequency-- in the communication.

Plasma is the yellowish liquid portion of whole blood that contains all clotting factors.. It is administered to treat bleeding disorders. Plasma extracted within 18 hours of donation is "fresh", but is then frozen to allow a 12 month shelf life.

Cardboard or plastic carton designed for use as a protective frame enhousing fresh frozen plasma bags during ultra low cryogenic storage

In this classification, this entry connotes a substrate made of Fructosamine that is used in clinical chemistry testing.

In this classification, this entry connotes a substrate made of Fructose that is used in clinical chemistry testing.

A tester that is designed to measure the resistance on the pressure of the fruit skin for quality management or confirmation on the level of ageing on fruit.

Is a device used to measure volumetric fuel consumption, that is, fuel volume passing through the fuel line per unit of time.

A tester that measures the contents of existing rubber substance in gasoline for vehicles or fuel for aircraft.

In this classification a fully automated short-term incubation cycle antimicrobial susceptibility system is a device that incorporates concentrations of antimicrobial agents into a system for the purpose of determining in vitro susceptibility of bacterial pathogens isolated from clinical specimens. Test results obtained from short-term (less than 16 hours) incubation are used to determine the antimicrobial agent of choice to treat bacterial diseases US FDA regulates Fully automated short-term incubation cycle antimicrobial susceptibility system under 21 CFR 866.1645 and under FDA product code LON.

An instrument designed and built to test parts and systems by emulating the operating envelope and requiring the test part to function as it would when used in the field.

Function generators are equipments which produce and provide various waveforms (Sign Wave, Pyramidal Wave, Square Wave, etc.) which satisfies given functional relations regarding time and voltage input.

In this classification, this entry connotes an extract made of Fungi used in an Immunological Allergenic test.

A measurement device that compares and inspects gauge block with the gauge block for master-level.

In this classification, this entry connotes a substrate made of Galactose that is used in clinical chemistry testing.

In this classification, Galactose-1-phosphate uridyl transferase test system connotes a device used to measure Galactose-1-phosphate uridyl transferase levels. US FDA regulates Galactose-1-phosphate uridyl transferase test system under 21 CFR 862.1315 and under FDA product code KQP.

In this classification, Galactose test system connotes a device used to measure Galactose levels. US FDA regulates Galactose test system under 21 CFR 862.1310 and under FDA product code JIA.

In this classification, this entry connotes a Gamma glutamyltransferase enzyme that is used in clinical chemistry testing.

In this classification, Gamma-glutamyl transpeptidase and isoenzymes test system connotes a device used to measure Gamma-glutamyl transpeptidase and isoenzymes levels. US FDA regulates Gamma-glutamyl transpeptidase and isoenzymes test system under 21 CFR 862.1360 and under FDA product code JPZ.

Equipment for gamma ray generation and survey that undertakes the non destructive inspection with respect to the interior defect of metal material.

In this classification, this entry connotes a colorimetric standard that incorporates the Gardner Color Index.

A gas chromatography column is a packed or capillary column used for separation and analysis on a gas chromatograph.

In this classification, a Gas-generating device connotes a device used intended for medical purposes that produces predetermined amounts of selected gases to be used in a closed chamber in order to establish suitable atmospheric conditions for cultivation of microorganisms with special atmospheric requirements. The device aids in the diagnosis of disease US FDA regulates Gas-generating device under 21 CFR 866.2580 and under FDA product code KZJ.

Automated system combining gas or liquid chromatography and mass spectrometry for sample constituent identifcation in diverse applications

Reagent or kit utilized for sample constituent identification in diverse applications by automated gas-liquid and/or mass spectrometry testing systems

In this classification a gas liquid chromatography system for clinical use is a device intended to separate one or more drugs or compounds from a mixture. Each of the constituents in a vaporized mixture of compounds is separated according to its vapor pressure US FDA regulates Gas liquid chromatography system for clinical use under 21 CFR 862.2250 and under FDA product code DLG.

In this classification, Gastric acidity test system connotes a device used to measure Gastric acidity levels. US FDA regulates Gastric acidity test system under 21 CFR 862.1320 and under FDA product code JLK.

In this classification, Gastrin test system connotes a device used to measure Gastrin levels. US FDA regulates Gastrin test system under 21 CFR 862.1325 and under FDA product code CGC.

A precision ground and lapped measuring standard. It is used as a reference for the setting or calibration of measuring equipment.

An exclusive gear tester that measures several errors of gear.

In this classification, a Gene expression profiling test system for breast cancer prognosis tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Gene expression profiling test system for breast cancer prognosis based tumors. US FDA regulates Gene expression profiling test system for breast cancer prognosis under 21 CFR 866.6040and under FDA product code NYI.

General field instruments are a broad category of devices that are commonly used to measure and monitor various physical and chemical parameters in industrial and process control applications. These instruments are designed to withstand harsh environmental conditions and provide accurate and reliable measurements in real-time and measure pressure, flow rate, temperature, and level, all of which are essential factors in plant operations.

In this classification a general purpose laboratory equipment labeled or promoted for a specific medical use is a device that is intended to prepare or examine specimens from the human body and that is labeled or promoted for a specific medical use US FDA regulates General purpose laboratory equipment labeled or promoted for a specific medical use under 21 CFR 862.2050 and under FDA product code LXG.

In this classification General purpose reagents are a chemical reagent that has general laboratory application, that is used to collect, prepare, and examine specimens from the human body for diagnostic purposes, and that is not labeled or otherwise intended for a specific diagnostic application. US FDA regulates General purpose reagents under 21 CFR 864.4010 and under FDA product code HZI.

Equipment that is designed to test the capability or function of power generator that generates electric energy.

Automated systems for qualitative and quantitative genomic analysis, gene expression, and polymerase chain reaction PCR amplification and detection

Replacement parts and accessories utilized on genomic analysis analyzers

In this classification, a Gentamicin test system is a device intended to measure Gentamicin for clinical toxicology purposes. US FDA regulates Gentamicin test system under 21 CFR 862.3450 and under FDA product code DJI

Glass equipment that has the bell-shape. It is used for combustion experiment to find out the properties of weight, ingredient and of air atmosphere.

A thermometer that uses the alcohol thermometer and the mercury thermometer, and measures maximum and minimum temperature.

In this classification, Globulin test system connotes a device used to measure Globulin levels. US FDA regulates Globulin test system under 21 CFR 862.1330 and under FDA product code CGH.

An instrument that measures the glossiness of material by measuring the sleekness and reflection rate of the material surface.

In this classification, Glucagon test system connotes a device used to measure Glucagon levels. US FDA regulates Glucagon test system under 21 CFR 862.1335 and under FDA product code JME.

In this classification, this entry connotes a substrate made of Glucose that is used in clinical chemistry testing.

Replacement parts and accessories for glucose test meters or monitors

In this classification, Glucose test system connotes a device used to measure Glucose levels. US FDA regulates Glucose test system under 21 CFR 862.1345 and under FDA product code NBW.

In this classification, this entry connotes a Glutamate dehydrogenase enzyme that is used in clinical chemistry testing.

In this classification a glutathione reductase assay is a device used to determine the activity of the enzyme glutathione reductase in serum, plasma, or erythrocytes by such techniques as fluorescence and photometry. The results of this assay are used in the diagnosis of liver disease, glutathione reductase deficiency, or riboflavin deficiency US FDA regulates Glutathione reductase assay under 21 CFR 864.7375 and under FDA product code KQF.

In this classification, Glutathione test system connotes a device used to measure Glutathione levels. US FDA regulates Glutathione test system under 21 CFR 862.1365 and under FDA product code JLN.

Monitor or meter for point of care glycosolated hemoglobin HBA1C analysis

Replacement parts and accessories for glycosolated hemoglobin HBA1c test meters

In this classification, this entry connotes a substrate made of Glycosylated/glycated hemoglobin that is used in clinical chemistry testing.

In this classification a glycosylated hemoglobin assay is a device used to measure the glycosylated hemoglobins (A1a, A1b, and A1c) in a patient's blood by a column chromatographic procedure. Measurement of glycosylated hemoglobin is used to assess the level of control of a patient's diabetes and to determine the proper insulin dosage for a patient. Elevated levels of glycosylated hemoglobin indicate uncontrolled diabetes in a patient US FDA regulates Glycosylated hemoglobin assay under 21 CFR 864.7470 and under FDA product code LCP.

In this classification, this entry connotes a reagent made of Gold chloride aqueous solution used in clinical chemistry testing.

A type of device that measures the size of the facial angle of the mineral crystal. The angle of a very small object can be measured by attaching mineral crystal to the semi-circular protractor and using the fixed bar and the moving bar.

In this classification, Gonococcal antibody test (gat) are devices used in test to identify specific Gonococcal antibody test (gat) antibodies in serum. US FDA regulates Gonococcal antibody test (gat) under 21 CFR 866.3290 and under FDA product code LGB.

In this classification, this entry connotes an extract made of Grama grass used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Grape used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Grass used in an Immunological Allergenic test.

A test that handles the friction, abrasion and lubrication of two sides that make contact and move around relatively.

A type of device that uses the electromagnetic wave, such as light, sound wave, radio electric wave and others as one of the geophysical prospecting method.

In this classification, this entry connotes an extract made of Gum used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Hackberry used in an Immunological Allergenic test.

In this classification, Haemophilus genus serological reagents are devices used in test to identify specific Haemophilus genus antibodies in serum. US FDA regulates Haemophilus genus serological reagents under 21 CFR 866.3300 and under FDA product code GRP.

A digital handheld single ocular microscope that allows for viewing of specimens or objects on a computer screen, as well as photographic or video capture, and has magnification powers of 10x to 150x

In this classification, a Haptoglobin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Haptoglobin. US FDA regulates Haptoglobin immunological test system under 21 CFR 866.5460 and under FDA product code DAD.

In this classification, this entry connotes an extract made of Hazelnut used in an Immunological Allergenic test.

A meter that measures the turbidity level when the light penetrates plastic film, plastic plate, glass plate and others.

A tester that inspects the capability of the tool that reinforces the hearing of the ear that has problem in hearing.

A tester that tests the degree of deformation when applying the heat to determine the stability following the temperature change on plastic, electric wire and rubber product.

A type of device that measures the heat movement volume by conduction, current or radiation by using the heat sensor.

A tester that is used for testing the capability and the operation condition of the heat sensor used in the fire facilities and others.

A meter for heating bills inspection that measures the heat consumption for each household as it is installed in common housing for central heating and local heating.

A tester that tests how well would the electric and electronic products endure under high temperature.

In this classification, a heat-sealing device is a device intended for medical purposes that uses heat to seal plastic bags containing blood or blood components. US FDA regulates Heat-sealing device under 21 CFR 864.9750 and under FDA product code KSD.

In this classification, Hematocrit measuring device connotes a system consisting of instruments, tubes, racks, and a sealer and a holder. The device is used to measure the packed red cell volume in blood to determine whether the patient's total red cell volume is normal or abnormal. Abnormal states include anemia (an abnormally low total red cell volume) and erythrocytosis (an abnormally high total red cell mass). The packed red cell volume is produced by centrifuging a given volume of blood. US FDA regulates Hematocrit measuring device under 21 CFR 864.6400 and under FDA product code JPI.

In this classification a hematology quality control mixture is a device used to ascertain the accuracy and precision of manual, semi automated, and automated determinations of cell parameters such as white cell count (WBC), red cell count (RBC), platelet count (PLT), hemoglobin, hematocrit (HCT), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), and mean corpuscular hemoglobin concentration (MCHC) US FDA regulates Hematology quality control mixture under 21 CFR 864.8625 and under FDA product code JPK.

In this classification, this entry connotes an extract made of Hemlock used in an Immunological Allergenic test.

Cover glass or slip utilized on hemocytometers or counting chambers that is constructed of a thicker and more high quality ground glass so that it is able to be disinfected and reused

In this classification a hemoglobin A2 assay is a device used to determine the hemoglobin A2 content of human blood. The measurement of hemoglobin A2 is used in the diagnosis of the thalassemias (hereditary hemolytic anemias characterized by decreased synthesis of one or more types of hemoglobin polypeptide chains) US FDA regulates Hemoglobin a2assay under 21 CFR 864.7400 and under FDA product code LGL.

In this classification, a Hemoglobin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Hemoglobin. US FDA regulates Hemoglobin immunological test system under 21 CFR 866.5470 and under FDA product code DAM.

Point of care rapid test meter for the measurement of hemoglobin or hematocrit in whole blood

In this classification, a Hemopexin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Hemopexin. US FDA regulates Hemopexin immunological test system under 21 CFR 866.5490 and under FDA product code CZX.

In this classification, this entry connotes an extract made of Hemp used in an Immunological Allergenic test.

In this classification a heparin assay is a device used to determine the level of the anticoagulant heparin in the patient's circulation. These assays are quantitative clotting time procedures using the effect of heparin on activated coagulation factor X (Stuart factor) or procedures based on the neutralization of heparin by protamine sulfate (a protein that neutralizes heparin) US FDA regulates Heparin assay under 21 CFR 864.7525 and under FDA product code KFF.

In this classification, Hepatitis a virus (hav) serological assays are devices used in test to identify specific Hepatitis a virus (hav) serological assays antibodies in serum. US FDA regulates Hepatitis a virus (hav) serological assays under 21 CFR 866.3310 and under FDA product code LOL.

In this classification, Herpes simplex virus serological assays are devices used in test to identify specific Herpes simplex virus serological assays antibodies in serum. US FDA regulates Herpes simplex virus serological assays under 21 CFR 866.3305 and under FDA product code GQN.

In this classification, this entry connotes an extract made of Hickory used in an Immunological Allergenic test.

In this classification, this entry connotes a substrate made of High density lipoprotein cholesterol that is used in clinical chemistry testing.

Portable cleaning equipment - any of a large class of implements used for cleaning.

Replaceable media placed before an HPLC column which provides contamination protection.

In this classification a high pressure liquid chromatography system for clinical use is a device intended to separate one or more drugs or compounds from a solution by processing the mixture of compounds (solutes) through a column packed with materials of uniform size (stationary phase) under the influence of a high pressure liquid (mobile phase) US FDA regulates High pressure liquid chromatography system for clinical use under 21 CFR 862.2260 and under FDA product code LDM.

A tester that measures the balance of the body of rotation in high speed. By rotating the body of rotation in high speed on the stand, the vertical shaft, it measures the location of the unbalance oscillation and the volume of oscillation as delivered to the bearing attached to the rotating shaft.

In this classification, Histidine test system connotes a device used to measure Histidine levels. US FDA regulates Histidine test system under 21 CFR 862.1375 and under FDA product code JMI.

Solvent and formalin resistant permanent markers for histology microslide and tissue cassette labeling

For prefilled 10% neutral buffered formalin specimen containers and other fixitives, media, and additives that are used for tissue collection and preservation for histology and pathology.

Tissue collection containers for histology and pathology that do not have an additive, media, or fixative.

Filing system for slides or cassettes.

Trays or racks composed of solvent resistant materials designed for the intermediate to long term storage of histology specimens in preservative filled containers

Accessories for histology equipment that include dividers, paper, pad, etc.

Hoppers used for the storage and dispensing of histology tissue cassettes

Tray or box that is used for the short or long term storage of histology tissue block cassettes

Ultra low temperature mechanically refrigerated bath utilized for the rapid freezing of histology tissue samples with minimal ice crystalization and faster freezing rate than cryostat or cryotome

All probes, brushes and other implements utilized in the dissection, embedding and microslide preparation of histological tissue for examination

Ultrasonic cleaner utilized in the histology laboratory for equipment cleaning and sample preparation such as bone specimen decalcification

In this classification, Histoplasma capsulatum serological reagents are devices used in test to identify specific Histoplasma capsulatum antibodies in serum. US FDA regulates Histoplasma capsulatum serological reagents under 21 CFR 866.3320 and under FDA product code GMJ.

A gauge that may precisely measure the inner diameter of small caliber in conjunction with the external diameter micrometer.

In this classification, this entry connotes an extract made of Hop used in an Immunological Allergenic test.

A scale of hopper type that automatically measures by dividing the weight of cargo in bulk condition for pulverulent body, particle, lump shaped agricultural and fishery products, raw material for industrial use, product and others.

Positive identification system of samples and reagents for hormones whether their origin is natural and or synthetic. Example: Triiodothyronine hormone T3 total for 200 determinations.

In this classification, this entry connotes an extract made of Horse epithelium used in an Immunological Allergenic test.

Test equipment station that contains equipment which monitors the performance of devices including engines and transmissions.  The device is hooked up to a test stand contained within the test station and all required fluids are supplied to start and run the device for an extended period of time.  The performance is then measured and recorded

In this classification, this entry connotes an extract made of House dust used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of House fly used in an Immunological Allergenic test.

In this classification, a Human allotypic marker immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Human allotypic marker. US FDA regulates Human allotypic marker immunological test system under 21 CFR 866.5065 and under FDA product code DHF.

In this classification, Human chorionic gonadotropin (hcg) test system connotes a device used to measure Human chorionic gonadotropin (hcg) levels. US FDA regulates Human chorionic gonadotropin (hcg) test system under 21 CFR 862.1155 and under FDA product code DHA.

In this classification, a Human epididymis protein 4 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Human epididymis protein 4 based tumors.

Granulocytes are white blood cells that fight infection through the immune response. They are obtained through donations via apheresis.

In this classification, Human growth hormone test system connotes a device used to measure Human growth hormone levels. US FDA regulates Human growth hormone test system under 21 CFR 862.1370 and under FDA product code CFL.

In this classification, a Human placenta like alkaline phosphatase tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Human placenta like alkaline phosphatase based tumors.

In this classification, Human placental lactogen test system connotes a device used to measure Human placental lactogen levels. US FDA regulates Human placental lactogen test system under 21 CFR 862.1585 and under FDA product code JMF.

Cellular component of whole blood

Human blood drawn directly from the body from which none of the components, such as plasma or platelets, has been removed. Whole blood is given through donation from one human to be administered to one of more recipients. Whole blood consists of red blood cells, white blood cells, and platelets suspended in a plasma.

Instrument for automatically controlling humidity in steaming cabinets and furnaces.

A type of device that is designed to test the capability of the device that measures humidity and the normal operation thereof.

A device which controls the humidity of the areas, such as laboratory and others.

A tester that tests the hydraulic formation of think plate. It is generally used in processing of narrow mouth impossible for mechanical press work or thin plate with thin thickness.

A device that tests the durability by applying the water pressure when confirming the condition of instrument, such as water pipe, tank, boiler, high pressure gas container and others with the applied pressure.

A tester which investigates the leakage or deformation by applying the hydraulic pressure to test the capability of pipe, tank and steam boiler.

In this classification, this entry connotes a standardized formulation of Hydrazine used to conduct Anion tests.

In this classification, this entry connotes a titrant of Hydrochloric acid used as a reagent in clinical chemistry testing.

A Hydrogen generator uses a proton exchange membrane (PEM) to produce high purity hydrogen gas from water. The PEM cell was originally developed by NASA and is extensively used in industrial and laboratory applications.

An instrument for detecting hydrogen sulfide in gas or oil.

A sound electric converter that reacts to the underwater sound energy to convert the energy into the intrinsically consistent (same) electric energy and stimulate the electric form factor, This machine is specially manufactured to use in water.

The performance of hydro processing reactors is determined not only by the catalyst loaded but also by the performance of their internals. Shell Catalysts & Technologies’ reactor internals technology uniformly distributes liquid and gas, minimizes thermal maldistribution, and maximizes catalyst volume and utilization.

Equipment that experiments how it is changed for rock or mineral of certain kind when the environment is set differently to the conditions of temperature and pressure at the time the rocks or minerals are generated.

In this classification, this entry connotes a Hydroxybutyrate dehydrogenase enzyme that is used in clinical chemistry testing.

In this classification, Hydroxybutyric dehydrogenase test system connotes a device used to measure Hydroxybutyric dehydrogenase levels. US FDA regulates Hydroxybutyric dehydrogenase test system under 21 CFR 862.1380 and under FDA product code JMK.

In this classification, Hydroxyproline test system connotes a device used to measure Hydroxyproline levels. US FDA regulates Hydroxyproline test system under 21 CFR 862.1400 and under FDA product code JMN.

Equipment that is used to determine the correction value of the scale inscribed on the hygrometer used for the measurement of humidity in atmosphere by adding the water into the chamber and heat it to change the humidity to 30 percent, 60 percent, and 90 percent.

In this classification, a Hypersensitivity pneumonitis immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Hypersensitivity pneumonitis. US FDA regulates Hypersensitivity pneumonitis immunological test system under 21 CFR 866.5500 and under FDA product code DGW.

A meter that measures the brightness of the reflector surface of light or the light source with certain width.

In this classification, Immunoelectrophoresis equipment connotes a device used to Immunoelectrophoresis is a procedure in which a complex protein mixture is placed in an agar gel and the various proteins are separated on the basis of their relative mobilities under the influence of an electric current. The separated proteins are then permitted to diffuse through the agar toward a multispecific antiserum, allowing precipitation and visualization of the separate complexes. US FDA regulates Immunoelectrophoresis equipment under 21 CFR 866.4500 and under FDA product code JZS.

In this classification, Immunofluorometer equipment connotes a device to measure the fluorescence of fluorochrome-labeled antigen-antibody complexes. The concentration of these complexes may be measured by means of reflected light. A beam of light is passed through a solution in which a fluorochrome has been selectively attached to serum protein antibody molecules in suspension. The amount of light emitted by the fluorochrome label is detected by a photodetector, which converts light energy into electrical energy. The amount of electrical energy registers on a readout system such as a digital voltmeter or a recording chart. This electrical readout is called the fluorescence value and is used to measure the concentration of antigen-antibody complexes. US FDA regulates Immunofluorometer equipment under 21 CFR 866.4520 and under FDA product code JZT.

In this classification, a Immunoglobulin g (fab fragment specific) immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Immunoglobulin g (fab fragment specific). US FDA regulates Immunoglobulin g (fab fragment specific) immunological test system under 21 CFR 866.5520 and under FDA product code DCE.

In this classification, a Immunoglobulin g (fc fragment specific) immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Immunoglobulin g (fc fragment specific). US FDA regulates Immunoglobulin g (fc fragment specific) immunological test system under 21 CFR 866.5530 and under FDA product code DBN.

In this classification, a Immunoglobulin g (fd fragment specific) immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Immunoglobulin g (fd fragment specific). US FDA regulates Immunoglobulin g (fd fragment specific) immunological test system under 21 CFR 866.5540 and under FDA product code DAQ.

In this classification, a Immunoglobulin (light chain specific) immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Immunoglobulin (light chain specific). US FDA regulates Immunoglobulin (light chain specific) immunological test system under 21 CFR 866.5550 and under FDA product code DAO.

In this classification, a Immunoglobulins a, g, m, d, and e immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Immunoglobulins a, g, m, d, and e. US FDA regulates Immunoglobulins a, g, m, d, and e immunological test system under 21 CFR 866.5510 and under FDA product code DAH.

Analyzer to automate all routine immunohematology testing procedures including blood grouping, reverse grouping, phenotyping, cross matching, antibody screening, antibody identification, direct AHG tests, and single antigen screens.

Accessories or supplies of analyzers for automating all routine immunohematology testing procedures including blood grouping, reverse grouping, phenotyping, cross matching, antibody screening, antibody identification, direct AHG tests, and single antigen screens

Reagents of analyzers to automate all routine immunohematology testing procedures including blood grouping, reverse grouping, phenotyping, cross matching, antibody screening, antibody identification, direct AHG tests, and single antigen screens

Quality controls or calibrators or standards for immunohematology testing procedures including blood grouping, reverse grouping, phenotyping, cross matching, antibody screening, antibody identification, direct AHG tests, and single antigen screens.

Immunohematology reagent or solution for ABO/Rh, antibody screening/identification and antigen typing

All autostainers utilized specificically for immunohistochemical special stain procedures

All IHC autostainer replacement parts, printing accessories, user defined dispensers and specialty slides

All quality control preserved tissue slides utilized specifically on IHC autostainers

In this classification, a Immunomagnetic circulating cancer cell selection and enumeration system tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Immunomagnetic circulating cancer cell selection and enumeration system based tumors. US FDA regulates Immunomagnetic circulating cancer cell selection and enumeration system under 21 CFR 866.6020 and under FDA product code NQI.

In this classification, Immunonephelometer equipment connotes a device used to that measures light scattering from antigen-antibody complexes. The concentration of these complexes may be measured by means of reflected light. A beam of light passed through a solution is scattered by the particles in suspension. The amount of light is detected by a photodetector, which converts light energy into electrical energy. The amount of electrical energy registers on a readout system such as a digital voltmeter or a recording chart. This electrical readout is called the light-scattering value and is used to measure the concentration of antigen-antibody complexes. This generic type of device includes devices with various kinds of light sources, such as laser equipment. US FDA regulates Immunonephelometer equipment under 21 CFR 866.4540 and under FDA product code JZW.

In this classification, Immunoreactive insulin test system connotes a device used to measure Immunoreactive insulin levels. US FDA regulates Immunoreactive insulin test system under 21 CFR 862.1405 and under FDA product code CFP.

An instrument used to check values of electrical components prior to final assembly allowing repair while electrical content is reduced.

A type of device that tests the temperature not to catch the fire to prevent the fire risk from textile product, electric wire, plastic, construction interior material, vehicle interior material and others.

A device that measures several data on indoor environment conservation of buildings in comprehensive terms. It may measure diversely in accordance with the device characteristics, such as indoor temperature, humidity, radiation temperature, wet bulb temperature, wind speed, relative humidity, carbon dioxide, carbon monoxide, dust and others.

A type of device that inspects with the oil pipe by lighting up the inside with flexible cable with the light inserted through a small hole of the outside without the machine or structure, such as engine, generator, duct, or elbow, disassembled.

An industrial radiograph viewing illuminator that is used for classification, grading and others of permeability photo that is obtained by the radiation permeability test by the X-ray, Gamma-ray and others.

In this classification, a Infectious mononucleosis immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Infectious mononucleosis. US FDA regulates Infectious mononucleosis immunological test system under 21 CFR 866.5640 and under FDA product code KTN.

In this classification, Influenza virus serological reagents are devices used in test to identify specific Influenza virus antibodies in serum. US FDA regulates Influenza virus serological reagents under 21 CFR 866.3330 and under FDA product code GNX.

A mark that is designed for navigation aid by using the infrared ray.

A device used to remotely measure temperature in situations where it is not possible to be in physical contact with the object being measured.This includes objects that are very hot, very small or very far away.

A sterile preparation of water, saline or propagation broth that is utilized to suspend bacterial or yeast primary culture colonies in solution for inoculation into identification or susceptibility panels

In this classification, this entry connotes a standardized formulation of Inorganic carbon used to conduct Anion tests.

In this classification, this entry connotes an extract made of Insect used in an Immunological Allergenic test.

Automated or robotic in situ sample surface harvester of cell cultures, providing standardization and uniformity of sampling

Runway Visual Range, or IRVR System provides an automated assessment of the distance an aircraft pilot can see the runway surface markings and lights.

In this classification Instrumentation for clinical multiplex test systems is a device intended to measure and sort multiple signals generated by an assay from a clinical sample. This instrumentation is used with a specific assay to measure multiple similar analytes that establish a single indicator to aid in diagnosis. Such instrumentation may be compatible with more than one specific assay. The device includes a signal reader unit, and may also integrate reagent handling, hybridization, washing, dedicated instrument control, and other hardware components, as well as raw data storage mechanisms, data acquisition software, and software to process detected signals US FDA regulates Instrumentation for clinical multiplex test systems under 21 CFR 862.2570 and under FDA product code NSU.

Insulated tote used for temperature controlled transport of biological specimens and products

In this classification, a Inter-alphatrypsin inhibitor immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Inter-alphatrypsin inhibitor. US FDA regulates Inter-alphatrypsin inhibitor immunological test system under 21 CFR 866.5890 and under FDA product code DEC.

In this classification, this entry connotes a device used to perform an In vitro human immunodeficiency virus (hiv) drug resistance genotype assay. US FDA regulates In vitro human immunodeficiency virus (hiv) drug resistance genotype assay under 21 CFR 866.3090 and under FDA product code NHS.

In this classification, this entry connotes a titrant of Iodate-iodide used as a reagent in clinical chemistry testing.

In this classification, this entry connotes a titrant of Iodate used as a reagent in clinical chemistry testing.

In this classification, this entry connotes a standardized formulation of Iodide used to conduct Anion tests.

In this classification, this entry connotes a titrant of Iodine used as a reagent in clinical chemistry testing.

Column for Ion chromatograph that separates samples into their constituent components.

Device that supports ion chromatography systems.

Replaceable media placed before an IC column which provides contamination protection.

A counter that is designed to measure a number of positive ion and negative ion in the air.

In this classification, this entry connotes a substrate made of Iron binding capacity that is used in clinical chemistry testing.

In this classification, Iron-binding capacity test system connotes a device used to measure Iron-binding capacity levels. US FDA regulates Iron-binding capacity test system under 21 CFR 862.1415 and under FDA product code JQF.

In this classification, Iron (non-heme) test system connotes a device used to measure Iron (non-heme) levels. US FDA regulates Iron (non-heme) test system under 21 CFR 862.1410 and under FDA product code CFM.

In this classification, this entry connotes a substrate made of Iron that is used in clinical chemistry testing.

In this classification, Isocitric dehydrogenase test system connotes a device used to measure Isocitric dehydrogenase levels. US FDA regulates Isocitric dehydrogenase test system under 21 CFR 862.1420 and under FDA product code JKH.

A device that may appraise and discern by detecting the optical and physical characteristics in various precious stones.

In this classification, this entry connotes an extract made of Juniper used in an Immunological Allergenic test.

In this classification, a Kanamycin test system is a device intended to measure Kanamycin for clinical toxicology purposes. US FDA regulates Kanamycin test system under 21 CFR 862.3520 and under FDA product code KXW

In this classification, Ketones (nonquantitative) test system connotes a device used to measure Ketones (nonquantitative) levels. US FDA regulates Ketones (nonquantitative) test system under 21 CFR 862.1435 and under FDA product code JIN.

Kit and reagent necessary for protein and/or nucleic acid gel agarose electrophoresis testing

Kit or reagent used to perform electrophoresis for quality control evaluation and purity analysis or quantitation of genomic DNA, DNA fragments and DNA libraries utilizing a tape based platform

In this classification, Klebsiella genus serological reagents are devices used in test to identify specific Klebsiella genus antibodies in serum. US FDA regulates Klebsiella genus serological reagents under 21 CFR 866.3340 and under FDA product code GTC.

Test tube and flask brushes and other brushes used to clean laboratory glassware

A type of laboratory animal housing and care equipment designed to catch and transport animals safely and humanely in a laboratory setting.

A mixer that is used for mixing the samples in a laboratory.

Wire, plastic, or rubber slings or racks used to safely transport laboratory bottles containing acids, solvents or caustic liquids

Special fitted bottle for filter pumps and filtration units.

Large capacity container, comprised of rigid plastic materials, that is used for the storage or transport of fluids and/or the spout utilized for dispensing from the carboy

A system which disrupts, homogenizes and/or emulsifies a specimen by ultrasonic vibration for the purpose of releasing biological molecules of a cell into suspension

A device that cures the cement mortar.

Consumables used in the laboratory are those items that must be replaced regularly when they are used or worn down. The types of labware include glassware, plasticware, and general lab supplies while the types of consumables include but are not limited to tubes, strips, filters, kits, reagents, caps, tips, gloves, and more. Laboratory chemicals refer to any chemical that's used in laboratory testing and experiments. Most are standard chemical reagents or simple chemicals that serve as basic ingredients to synthesize more complex chemicals

Equipment assigned to the cutting of substances used in the laboratory.

Flask utilized for the storage of liquid nitrogen used in laboratory cryogenic freezers, that is insulated by a double wall with vacuum between the walls and silvered surfaces facing the vacuum

Bottles and bottle caps utilized specifically for dropper dispensing of reagents and solutions

Equipment that supplies the solid, liquid, and vapor phases consecutively and automatically from the laboratory.

Used for separating different substances of different physical states.

It is a type of fractional distillation that is specially undertaken when classifying the solution that contains two or more kinds of volatile ingredient, such as alcohol, perfume, petroleum and the like, for each ingredient. The fraction is the measurement of substance capacity lessened within the scope of regulated temperature and this device enables to measure such classification and quantity.

Equipment that generates the pertinent gases required in the experiment at the laboratories. It has different configuration or types for each gas generated thereof.

General purpose heat sealer used for sealing bags within the laboratory

A base glass that makes the glass device for testing, such as test tube, or cylinder. The coefficient of thermal expansion is low that there is almost no impact by the heat expansion during the experiment.

A device used to seamlessly grind or finely process the surface of glassware or a test article.

A metal pot used with mineral grinders or pulverizers. It has adjustment rings.

Thermometer used for critical temperature monitoring in laboratory heat blocks

A type of sintering equipment that uses the densification of the ceramic powder and others that would be unable to manufacture with the dissolution method for high fusion point in using high temperature and high pressure simultaneously.

These are covers and lids for beakers, flasks, graduated cylinders, etc.

Thermometer used for critical temperature monitoring in laboratory ovens

A type of device that undertakes the chemical or biological reaction from the laboratory. This device is to make the chemical reaction easier by giving the time to stay or add the heat, pressure, agitation, light or catalyst.

Scoop used within the laboratory for dispensing solid materials

Screening test is done to detect potential health disorders or diseases in people who do not have any symptoms of disease. The goal is early detection and lifestyle changes or surveillance, to reduce the risk of disease, or to detect it early enough to treat it most effectively. Kit also contains primers and probes.

Spoons for general laboratory material dispersal.

General purpose over-the-sink stain racks and trays

A device used to generate steam needed in the laboratory.

Bottles utilized for media and general storage

Decontamination agent used for labware and laboratory surfaces to remove biological, chemical and nucleic acid contamination

Wax compound used for forming a leak tight seal for tubes.

A laboratory variant of membrane filtration equipment in which forces like pressure or concentration gradients lead to a separation through a semipermeable membrane.

A type of portable inspection device that is used in observation for the defect on the surface by shedding the ultraviolet rays with the built-in light source.

Process equipment that is designed to dispose the reaction compounds or residues after the use at the laboratory.

Thermometer used for critical temperature monitoring in laboratory water baths

An experiment device that is used for the analysis and adjustment of waves. Motor and linear motion system cause the wave and this device is for the experiment to find out how the object, like a boat floating on fluid, could react to the wave or impact of tidal wave or wave on the dike.

Control equipment that is designed for the X-ray detector. It controls the X-ray device to maintain the optimal condition to detect the material or part defect.

Screening test is done to detect potential health disorders or diseases in people who do not have any symptoms of disease. The goal is early detection and lifestyle changes or surveillance, to reduce the risk of disease, or to detect it early enough to treat it most effectively. Kit also contains primers and probes.

In this classification, this entry connotes a substrate made of Lactate that is used in clinical chemistry testing.

In this classification, this entry connotes a Lactate dehydrogenase isoenzymes enzyme that is used in clinical chemistry testing.

In this classification, Lactate dehydrogenase isoenzymes test system connotes a device used to measure Lactate dehydrogenase isoenzymes levels. US FDA regulates Lactate dehydrogenase isoenzymes test system under 21 CFR 862.1445 and under FDA product code CFE.

In this classification, this entry connotes a Lactate dehydrogenase l enzyme that is used in clinical chemistry testing.

In this classification, this entry connotes a Lactate dehydrogenase p enzyme that is used in clinical chemistry testing.

In this classification, Lactate dehydrogenase test system connotes a device used to measure Lactate dehydrogenase levels. US FDA regulates Lactate dehydrogenase test system under 21 CFR 862.1440 and under FDA product code CFJ.

In this classification, Lactic acid test system connotes a device used to measure Lactic acid levels. US FDA regulates Lactic acid test system under 21 CFR 862.1450 and under FDA product code KHP.

In this classification, a Lactic dehydrogenase immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Lactic dehydrogenase. US FDA regulates Lactic dehydrogenase immunological test system under 21 CFR 866.5560 and under FDA product code DET.

In this classification, a Lactoferrin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Lactoferrin. US FDA regulates Lactoferrin immunological test system under 21 CFR 866.5570 and under FDA product code DEG.

In this classification, a Laminin tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Laminin based tumors.

A tester that tests a number of characteristics on life cycle of fluorescent lamp, incandescent lamp, light-emitting diode lamp and others or power efficiency, brightness, temperature change and others.

An instrument that monitors yaw or side-to-side movement from a given axis.

An LCR meter is a type of electronic test equipment used to measure the inductance (L), capacitance (C), and resistance (R) of an electronic component.

A type of device that is used for surveying. It is the line with the scale and it is generally made for steel chain, hemp yarn, cotton yarn, glass fiber and others, and it hangs the weight made by iron or lead at the end of the line.

In this classification, a Lead test system is a device intended to measure Lead for clinical toxicology purposes. US FDA regulates Lead test system under 21 CFR 862.3550 and under FDA product code DOF

A meter that measures the accurate leaf area with the luminescence method to analyze with the sensor by penetrating the light on the opaque and irregular plant leaf with the built-in camera focus.

In this classification, this entry connotes a substrate made of Lecithin that is used in clinical chemistry testing.

In this classification, Lecithin/sphingomyelin ratio in amniotic fluid test system connotes a device used to measure Lecithin/sphingomyelin ratio in amniotic fluid levels. US FDA regulates Lecithin/sphingomyelin ratio in amniotic fluid test system under 21 CFR 862.1455 and under FDA product code JHG.

In this classification, lectins and protectins are proteins derived from plants and lower animals that cause cell agglutination in the presence of certain antigens. These substances are used to detect blood group antigens for in vitro diagnostic purposes. US FDA regulates Lectins and protectins under 21 CFR 864.9550 and under FDA product code KSI.

In this classification, Leptospira genus serological reagents are devices used in test to identify specific Leptospira genus antibodies in serum. US FDA regulates Leptospira genus serological reagents under 21 CFR 866.3350 and under FDA product code GRY.

In this classification, this entry connotes an extract made of Lettuce used in an Immunological Allergenic test.

In this classification, this entry connotes a Leucine aminopeptidase enzyme that is used in clinical chemistry testing.

In this classification, Leucine aminopeptidase test system connotes a device used to measure Leucine aminopeptidase levels. US FDA regulates Leucine aminopeptidase test system under 21 CFR 862.1460 and under FDA product code JGG.

In this classification a leukocyte alkaline phosphatase test is a device used to identify the enzyme leukocyte alkaline phosphatase in neutrophilic granulocytes (granular leukocytes stainable by neutral dyes). The cytochemical identification of alkaline phosphatase depends on the formation of blue granules in cells containing alkaline phosphatase. US FDA regulates Leukocyte alkaline phosphatase test under 21 CFR 864.7660 and under FDA product code GHD.

In this classification a leukocyte peroxidase test is a device used to distinguish certain myeloid cells derived from the bone marrow, i.e., neutrophils, eosinophils, and monocytes, from lymphoid cells of the lymphatic system and erythroid cells of the red blood cell series on the basis of their peroxidase activity as evidenced by staining US FDA regulates Leukocyte peroxidase test under 21 CFR 864.7675 and under FDA product code GIA.

There are various types of level indicators: one type is a bead type, some are of visible transparent material, some are of float type.

In this classification, a Lidocaine test system is a device intended to measure Lidocaine for clinical toxicology purposes. US FDA regulates Lidocaine test system under 21 CFR 862.3555 and under FDA product code KLR

Agglutination viewer that consists of a glare-free backlighting source for use with blood bank or other applications where magnification is not necessary

Agglutination viewer that consists of an under placed magnifying mirror and above placed light to allow for undersurface observation of universal flocculation reactions

A large scale spark discharge in air that occurs in nature is referred to as the lightning or thunder. This is equipment that is used to expect the storm and others by sensing the quantity of electric discharge and its location in the convective cloud.

A tester that obtains an aqueous extract of blood cells (amebocytes) from the horseshoe crab, Limulus polyphemus.

In this classification, this entry connotes an extract made of Linden used in an Immunological Allergenic test.

A type of device that is installed and used in the high voltage equipment or high voltage conductor.

In this classification, this entry connotes a Lipase enzyme that is used in clinical chemistry testing.

In this classification, Lipase test system connotes a device used to measure Lipase levels. US FDA regulates Lipase test system under 21 CFR 862.1465 and under FDA product code CHI.

Monitor or meter utilized for point of care whole blood lipid profile and "at risk" liver enzymes analysis

Replacement parts and accessories utilized for point of care whole blood lipid profile and "at risk" liver enzymes analysis

In this classification, Lipid (total) test system connotes a device used to measure Lipid (total) levels. US FDA regulates Lipid (total) test system under 21 CFR 862.1470 and under FDA product code CFB.

In this classification, this entry connotes a substrate made of Lipoprotein, chemical determination/detection that is used in clinical chemistry testing.

In this classification, this entry connotes a substrate made of Lipoprotein electrophoresis that is used in clinical chemistry testing.

In this classification, Lipoprotein test system connotes a device used to measure Lipoprotein levels. US FDA regulates Lipoprotein test system under 21 CFR 862.1475 and under FDA product code JHM.

In this classification, a Lipoprotein x immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Lipoprotein x. US FDA regulates Lipoprotein x immunological test system under 21 CFR 866.5590 and under FDA product code DEL.

Device that supports liquid chromatography systems.

Flexible stick, usually constructed from fiberglass, that is utilized for measuring the level of liquid nitrogen in storage tanks or systems

A type of device that is designed to measure the liquid ratio of each ingredient for mixed liquid after mixing two or more of liquids of mutually different character and condition.

In this classification, Listeria genus serological reagents are devices used in test to identify specific Listeria genus antibodies in serum. US FDA regulates Listeria genus serological reagents under 21 CFR 866.3355 and under FDA product code GSI.

In this classification, a Lithium test system is a device intended to measure Lithium for clinical toxicology purposes. US FDA regulates Lithium test system under 21 CFR 862.3560 and under FDA product code JII

Equipment that is designed to measure the load working on the structure. This is the load tester of flexural fracture for pressed cement roof tile or fiber reinforced cement boards.

In this classification, this entry connotes an extract made of Lobster used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Locust used in an Immunological Allergenic test.

In this classification, this entry connotes a substrate made of Low density lipoprotein cholesterol including sd-ldl that is used in clinical chemistry testing.

In this classification, a Low-density lipoprotein immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Low-density lipoprotein. US FDA regulates Low-density lipoprotein immunological test system under 21 CFR 866.5600 and under FDA product code DFC.

A type of device that warns in real time if the meteorological data detected by the turbulence arising from the layer near to the earth surface --planetary boundary layer-- exceeds the range of set value.

A tester that is designed to test the capability of large device under the alternating current of 600V or less and, the direct current of 750V or less.

In this classification, Luteinizing hormone test system connotes a device used to measure Luteinizing hormone levels. US FDA regulates Luteinizing hormone test system under 21 CFR 862.1485 and under FDA product code CEP.

A device used to measure the amount of light. In photography, a light meter (more correctly an exposure meter) is used to determine the proper exposure for a photograph.

In this classification a lymphocyte separation medium is a device used to isolate lymphocytes from whole blood US FDA regulates Lymphocyte separation medium under 21 CFR 864.8500 and under FDA product code JCF.

In this classification, Lymphocytic choriomeningitis virus serological reagents are devices used in test to identify specific Lymphocytic choriomeningitis virus antibodies in serum. US FDA regulates Lymphocytic choriomeningitis virus serological reagents under 21 CFR 866.3360 and under FDA product code GQK.

In this classification, a Lysergic acid diethylamide (lsd) test system is a device intended to measure Lysergic acid diethylamide (lsd) for clinical toxicology purposes. US FDA regulates Lysergic acid diethylamide (lsd) test system under 21 CFR 862.3580 and under FDA product code DOL

In this classification, this entry connotes a Lysozyme enzyme that is used in clinical chemistry testing.

In this classification, Lysozyme (muramidase) test system connotes a device used to measure Lysozyme (muramidase) levels. US FDA regulates Lysozyme (muramidase) test system under 21 CFR 862.1490 and under FDA product code JMR.

A device used to melt magnesium pellets or balls for further processing.

In this classification, Magnesium test system connotes a device used to measure Magnesium levels. US FDA regulates Magnesium test system under 21 CFR 862.1495 and under FDA product code JGI.

A magnet and a magnetic field detector that have the warning (alarm) functions if there are any magnetic field present, scope of its strength, and certain strength.

A magnetic level gauge is a type of level sensor, i.e., a device used to measure the level of fluids, A magnetic level gauge includes a “floatable” device that can float both in high and low density fluids. Magnetic level gauges may also be designed to accommodate severe environmental conditions up to 210 bars at 370 °C.

In this classification, this entry connotes a Malate dehydrogenase enzyme that is used in clinical chemistry testing.

In this classification, Malic dehydrogenase test system connotes a device used to measure Malic dehydrogenase levels. US FDA regulates Malic dehydrogenase test system under 21 CFR 862.1500 and under FDA product code JMS.

In this classification, Manual blood cell counting device connotes a device used to count red blood cells, white blood cells, or blood platelets. US FDA regulates Manual blood cell counting device under 21 CFR 864.6160 and under FDA product code GKM.

Subculture devices utilized for manual processing of blood and body fluid cultures inoculated into blood culture bottles

In this classification, a Manual colony counter connotes a device used for the manual counting colonies of bacteria growing in a culture. US FDA regulates Manual colony counter under 21 CFR 866.2180 and under FDA product code KZC.

Device for manual reading and measurement of blood hematocrit level from spun microhematocrit tubes

The nosepiece or turret, which has manual rotation, that holds two or more objective lenses on a microscope

In this classification, this entry connotes an extract made of Maple used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Marshelder used in an Immunological Allergenic test.

In this classification a mass spectrometer for clinical use is a device intended to identify inorganic or organic compounds (e.g., lead, mercury, and drugs) in human specimens by ionizing the compound under investigation and separating the resulting ions by means of an electrical and magnetic field according to their mass US FDA regulates Mass spectrometer for clinical use under 21 CFR 862.2860 and under FDA product code DOP.

In this classification, this entry connotes a standardized preparation made of Matching fluid a, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid b, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid c, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid d, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid e, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid f, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid g, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid h, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid i, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid j, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid k, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid l, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid m, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid n, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid o, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid p, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid q, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid r, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid s, used in a colorimetric Clinical laboratory test.

In this classification, this entry connotes a standardized preparation made of Matching fluid t, used in a colorimetric Clinical laboratory test.

In this classification, a Matrix-metalloproteinases tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Matrix-metalloproteinases based tumors.

Equipment that is designed to convert into the same type or different type of signal or volume for responding to the signal or volume thereof.

An apparatus that makes and sterilizes the culture solution to culture the germs, and injects this culture solution into the petri dish for certain volume at a time.

An instrument that is used to measures the melting point, namely, the temperature that a substance changes its phase from the solid state to the liquid state.

In this classification, this entry connotes a titrant of Mercuric nitrate used as a reagent in clinical chemistry testing.

An analyzer that measures the ingredient of mercury included in tap water, sea water, flood, urine, heavy oil, soil, food, exhaust gas or atmosphere.

In this classification, a Mercury test system is a device intended to measure Mercury for clinical toxicology purposes. US FDA regulates Mercury test system under 21 CFR 862.3600 and under FDA product code DPH

Point of care rapid test meter for the measurement of single or multiple parameters in the detection of metabolic disorders from breath specimens

A weather balloon, also known as sounding balloon, is a balloon that carries instruments aloft to send back information on atmospheric pressure, temperature, humidity and wind speed by means of a small, expendable measuring device called a radiosonde.

A type of device that has the function to forward the result of meteorology and marine observation on the sea to the land via wireless communication in real time.

A system that processes and analyzes the meteorological data by receiving the data sent by the satellite (climate satellite) that loads the meteorological instruments. It is structured with antenna, receiver, processor and analyzer (computer).

A system that outputs the meteorological chart through monitor and printer for the editing function through the computer by automatically receiving the photo taken by the artificial satellite that is sent to observe the meteorological condition on earth. It is structured with the receiving equipment for meteorological satellite image and the data processing device.

A type of radar that is used in detecting the meteorology phenomenon. Rain, snow, and cloud consisted of water drop or ice crystal reflects the electric wave that it may detect the collective bodies in typhoon, thunderstorm, front and others.

In this classification, a Methadone test system is a device intended to measure Methadone for clinical toxicology purposes. US FDA regulates Methadone test system under 21 CFR 862.3620 and under FDA product code DJR

In this classification, a Methamphetamine test system is a device intended to measure Methamphetamine for clinical toxicology purposes. US FDA regulates Methamphetamine test system under 21 CFR 862.3610 and under FDA product code LAF

In this classification, a Methaqualone test system is a device intended to measure Methaqualone for clinical toxicology purposes. US FDA regulates Methaqualone test system under 21 CFR 862.3630 and under FDA product code KXS

In this classification, Methylmalonic acid (nonquantitative) test system connotes a device used to measure Methylmalonic acid (nonquantitative) levels. US FDA regulates Methylmalonic acid (nonquantitative) test system under 21 CFR 862.1509 and under FDA product code LPT.

A growth system, consisting of a pouch or bag and gas generator, that provides an environment rich in carbon dioxide to promote optimal growth conditions for isolating Campylobacter jejuni, and which allows direct observation of the media plate without disruption of that microaerophilic environment

In this classification, a Microbial growth monitor connotes a device used for medical purposes that measures the concentration of bacteria suspended in a liquid medium by measuring changes in light scattering properties, optical density, electrical impedance, or by making direct bacterial counts. The device aids in the diagnosis of disease caused by pathogenic microorganisms US FDA regulates Microbial growth monitor under 21 CFR 866.2560 and under FDA product code JTA.

A single microbial organism that is guaranteed traceable back to a known type culture with usually less than five subcultures or passes, which has been lyophilized to be rehydrated and grown for future use as a quality control in multiple method validations in microbiology, and will be utilized as a constituent of laboratory accrediation

Desiccated containers utilized for the storage of Microbial susceptibility disc storage

In this classification, a Microbiological assay culture medium connotes a device that consists primarily of liquid or solid biological materials intended for medical purposes to cultivate selected test microorganisms in order to measure by microbiological procedures the concentration in a patient's serum of certain substances, such as amino acids, antimicrobial agents, and vitamins US FDA regulates Microbiological assay culture medium under 21 CFR 866.2350 and under FDA product code JSA.

In this classification, a Microbiological incubator connotes a device used to grow and maintain microbiological cultures or cell cultures. The incubator maintains optimal temperature, humidity and other conditions such as the carbon dioxide (CO2) and oxygen content of the atmosphere inside US FDA regulates Microbiological incubator under 21 CFR 866.2540 and under FDA product code JTQ.

In this classification, a Microbiological specimen collection and transport device connotes a device used as a specimen collecting chamber intended for medical purposes to preserve the viability or integrity of microorganisms in specimens during storage of specimens after their collection and during their transport from the collecting area to the laboratory. US FDA regulates Microbiological specimen collection and transport device under 21 CFR 866.2900 and under FDA product code LIO.

In this classification a micro chemistry analyzer for clinical use is a device intended to duplicate manual analytical procedures by performing automatically various steps such as pipetting, preparing filtrates, heating, and measuring color intensity. The distinguishing characteristic of the device is that it requires only micro volume samples obtainable from pediatric patients US FDA regulates Micro chemistry analyzer for clinical use under 21 CFR 862.2170 and under FDA product code JJF.

A type of device that is used by attaching to the microscope. It sets the tools, such as micro-pipet, finite cutter, finite injector and others, to have the finite maneuvering of cells, nuclear transplant, electric stimulation, cutting and others.

In this classification, a Microorganism differentiation and identification device connotes a device used intended for medical purposes that consists of one or more components, such as differential culture media, biochemical reagents, and paper discs or paper strips impregnated with test reagents, that are usually contained in individual compartments and used to differentiate and identify selected microorganisms. The device aids in the diagnosis of disease US FDA regulates Microorganism differentiation and identification device under 21 CFR 866.2660 and under FDA product code JTO.

Shaker, specific to microplates, that has orbital, reciprocal or rotating action to maintain homogenous mixture within contents of microplate wells

Table or mat that is designed to protect microscopes, their components and clinical specimens for microscopic examination from external oscillations or vibrations

The bottom aspect of a microscope, utilized to support the viewing elements of that microscope

The basic structural aspect of the microscope, which includes the eyepiece and objective lenses, but does not include the base, illuminators or focusing block

Cleaning kit utilized for preventive maintenance of microscopes

Equipment that uses the interference effect of light to display the object shown on plane to show the sense of dimension with the height by installing the prism corresponding to each multi-ratio of the objective lens on the condenser.

Box or cube which houses spectral imaging filters for fluorescent microscopes

Any replacement screw, clamp, adapter or other fitting utilized on microscope

Excitation, emission, or dichroic filter utilized for coordinating spectral chromophores in fluorescent microscopes

The upper part of the microscope that contains a one or two eyepiece lenses and prisms, and which attaches to the tube, generally referred to with compound light microscopes

Knob that is used for coarse and fine vertical adjustment of the objectives and condenser of a microscope, or that is used for the horizontal and vertical adjustment of the microscope stage for optimal viewing of specimens

Cleaning solutions for the maintenance of microscope lenses and objectives

A pointer within the eyepiece of the microscope that allows the viewer to reference a particular part of a specimen being observed and which can be moved by rotating the eyepiece

System and accessories that are mechanical and/or interfaced to be utlized with a microscope or multiple microscopes for manipulation of samples being observed

In this classification microscopes and accessories are devices and their accessories that are an optical instrument having a magnifying lens or a combination of lenses for inspecting objects too small to be seen or too small to be seen distinctly and in detail by the unaided eye US FDA regulates Microscopes and accessories under 21 CFR 864.36 and under FDA product code KEH.

All reference markers or specimen tracker cards or position end supports for microscope slide or histology cassette storage cabinets

Adjustable clip utilized to entrap and stabilize microscope slides on the stage of a microscope

A warming system or microincubator that rests on the stage of inverted microscopes and allows for in vivo observation of cell culture without disruption of growth environment

A meter that is used to measure the finite size of object by using the microscope. There are ocular and objective lens.

In this classification, a amicrosedimentation centrifuge is a device used to sediment red cells for the microsedimentation rate test. US FDA regulates Microsedimentation centrifuge under 21 CFR 864.5350 and under FDA product code GHK.

In this classification, a Microtiter diluting and dispensing device connotes a mechanical device intended for medical purposes to dispense or serially dilute very small quantities of biological or chemical reagents for use in various diagnostic procedures US FDA regulates Microtiter diluting and dispensing device under 21 CFR 866.2500 and under FDA product code JTC.

In this classification a microtitrator for clinical use is a device intended for use in micronanalysis to measure the concentration of a substance by reacting it with a measure "micro" volume of a known standardized solution US FDA regulates Microtitrator for clinical use under 21 CFR 862.2680 and under FDA product code JRA.

A tester that is designed for experiment as composed with microwave transmitter and receiver and other auxiliary part. This is a device composed to undertake reflected, ordinary wave experiment and others.

In this classification, this entry connotes an extract made of Milk used in an Immunological Allergenic test.

A type of device that specifically analyzes the fat, protein, milk sugar, fat-free dry matter and others in the milk. This device generally uses the wavelength of the infrared ray to sense the light from the special wavelength territory for the quantitative analysis of the ingredient.

In this classification, this entry connotes an extract made of Millet used in an Immunological Allergenic test.

Equipment that continuously observes the process of nurturing and growth through the entire nurturing period of the root under the soil for the plant.

A type of optical instrument that reads the actual body as photo, map and object are expanded for better view.

In this classification, this entry connotes an extract made of Mite used in an Immunological Allergenic test.

In this classification, this entry connotes a standardized formulation of Mixed anion used to conduct Anion tests.

In this classification, this entry connotes an extract made of Mold used in an Immunological Allergenic test.

All growth media for cell and tissue culture utilized to facilitate molecular biological evaluations

Automated system for qualitative and quantitative nucleic acid diagnostics

Replacement parts and accessories for molecular diagnostics automated testing system

Reagents for molecular diagnostics automated testing system

A material device containing tiny pores of a precise and uniform size that is used as an adsorbent for gases and liquids.Molecules small enough to pass through the pores are adsorbed while larger molecules are not. It differs from a common filter in that it operates on a molecular level.

All controls, calibrators and standards utilized in maintaining accurate linearity of point of care test meters

In this classification, this entry connotes an extract made of Monkey dander used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Monkey hair used in an Immunological Allergenic test.

In this classification, a Morphine test system is a device intended to measure Morphine for clinical toxicology purposes. US FDA regulates Morphine test system under 21 CFR 862.3640 and under FDA product code DJJ

In this classification, this entry connotes a standardized formulation of Morpholine used to conduct Anion tests.

A tester that measures the length change of the mortar following the volume of water to make the mortar with certain properties.

A tester that measures permeable volume and permeable ratio by applying the pressure with water on the mortar or cement for construction.

The nosepiece or turret, which has motorized rotation, that holds two or more objective lenses on a microscope

In this classification, Mucopolysaccharides (nonquantitative) test system connotes a device used to measure Mucopolysaccharides (nonquantitative) levels. US FDA regulates Mucopolysaccharides (nonquantitative) test system under 21 CFR 862.1505 and under FDA product code JQN.

In this classification, this entry connotes an extract made of Mugwort used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Mulberry used in an Immunological Allergenic test.

Manual slide stainer sets with containers and racks that are user defined for use in multiple department staining procddures

A microscope that includes the video analysis system.

Hand held multimeter that senses readings by clamping on or around wiring.

Medical device that typically contains a sensor for capturing important patient information (e.g., heart rate) and an interconnect solution. It is mainly used in intensive care, hospitalization or ER.

Medical device that typically contains a sensor for capturing important patient information (e.g., heart rate) and an interconnect solution. It is mainly used in intensive care, hospitalization or ER

In this classification, a Multiple autoantibodies immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Multiple autoantibodies. US FDA regulates Multiple autoantibodies immunological test system under 21 CFR 866.5660 and under FDA product code DBL.

Automated systems for simultaneous qualitative and quantitative multiplex microarry analysis

Replacement parts and accessories utilized on multiplex analyzers

In this classification, a Multipurpose culture medium connotes a device that consists primarily of liquid or solid biological materials intended for medical purposes for the cultivation and identification of several types of pathogenic microorganisms without the need of additional nutritional supplements US FDA regulates Multipurpose culture medium under 21 CFR 866.2300 and under FDA product code JSB.

In this classification, a multipurpose system for in vitro coagulation studies is a device consisting of one automated or semi automated instrument and its associated reagents and controls. The system is used to perform a series of coagulation studies and coagulation factor assays. US FDA regulates Multipurpose system for in vitro coagulation studies under 21 CFR 864.5425 and under FDA product code JPA.

In this classification, Mumps virus serological reagents are devices used in test to identify specific Mumps virus antibodies in serum. US FDA regulates Mumps virus serological reagents under 21 CFR 866.3380 and under FDA product code GRC.

In this classification, this entry connotes an extract made of Mushroom used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Mustard used in an Immunological Allergenic test.

In this classification, Mycobacterium tuberculosis immunofluorescent reagents are devices used in test to identify specific Mycobacterium tuberculosis immunofluorescent reagents antibodies in serum. US FDA regulates Mycobacterium tuberculosis immunofluorescent reagents under 21 CFR 866.3370 and under FDA product code GRT.

In this classification, mycoplasma detection media and components are used to detect and isolate mycoplasma pleuropneumonia-like organisms (PPLO), a common microbial contaminant in cell cultures. US FDA regulates Mycoplasma detection media and components under 21 CFR 864.2360 and under FDA product code KIX.

In this classification, Mycoplasma genus serological reagents are devices used in test to identify specific Mycoplasma genus antibodies in serum. US FDA regulates Mycoplasma genus serological reagents under 21 CFR 866.3375 and under FDA product code GSB.

In this classification, a Myoglobin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Myoglobin. US FDA regulates Myoglobin immunological test system under 21 CFR 866.5680 and under FDA product code DDR.

In this classification, this entry connotes a N-acetyl-b,d-glucosaminidase enzyme that is used in clinical chemistry testing.

PCR device for rapid DNA amplification and detection.

In this classification, Neisseria genus direct serological test reagents are devices used in test to identify specific Neisseria genus direct serological test reagents antibodies in serum. US FDA regulates Neisseria genus direct serological test reagents under 21 CFR 866.3390 and under FDA product code LIR.

Filter cards used in the collection and transport of neonatal blood samples for state mandated metabolic disorder screening

In this classification a nephelometer for clinical use is a device intended to estimate the concentration of particles in a suspension by measuring their light scattering properties (the deflection of light rays by opaque particles in their path). The device is used in conjunction with certain materials to measure the concentration of a variety of analytes US FDA regulates Nephelometer for clinical use under 21 CFR 862.270 and under FDA product code JQX.

In this classification, a Neuroleptic drugs radio receptor assay test system is a device intended to measure Neuroleptic drug radio receptors for clinical toxicology purposes. US FDA regulates Neuroleptic drugs radio receptor assay test system under 21 CFR 862.3645 and under FDA product code KLT

In this classification, a Neuron specific enolase tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Neuron specific enolase based tumors.

Neutron has fine substance permeability for not having the electric charge. It is used It is used for the internal crystal structure study of substance, inspection of defective part or inspection of plastic or chemicals with the method of obtaining the penetration film of heat neutron by using the nuclear furnace of neutron source. This is the generating device of neutron thereof.

In this classification, Newborn screening test system for amino acids, free carnitine, and acylcarnitines using tandem mass spectrometry connotes a device used to measure Newborn screening for amino acids, free carnitine, and acylcarnitines using tandem mass spectrometry levels. US FDA regulates Newborn screening test system for amino acids, free carnitine, and acylcarnitines using tandem mass spectrometry under 21 CFR 862.1055 and under FDA product code NQL.

In this classification, this entry connotes a standardized formulation of Nitrate used to conduct Anion tests.

In this classification, Nitrite (nonquantitative) test system connotes a device used to measure Nitrite (nonquantitative) levels. US FDA regulates Nitrite (nonquantitative) test system under 21 CFR 862.1510 and under FDA product code JMT.

In this classification, this entry connotes a standardized formulation of Nitrite used to conduct Anion tests.

In this classification, Nitrogen (amino-nitrogen) test system connotes a device used to measure Nitrogen (amino-nitrogen) levels. US FDA regulates Nitrogen (amino-nitrogen) test system under 21 CFR 862.1515 and under FDA product code JMW.

In this classification, this entry connotes a standardized formulation of Nitrogen used to conduct Anion tests.

A type of device that generates certain noise for using on the level calibration of extremely short wavelength with noise factor and others or noise loading tester.

A meter that is designed to measure the noise level of the circuit. Since the circuit for weight addition for appropriate frequency and other required functions are added, this device may mark what noise may cause how much interference thereof.

In this classification, this entry connotes a titrant of Nonaqueous used as a reagent in clinical chemistry testing.

A chemical that is used in non-destructive examination. It is appropriate to the penetration inspection, and when testing all solid surfaces, it detects the material defect open on the surface.

In this classification, this entry connotes a substrate made of Non esterified fatty acids that is used in clinical chemistry testing.

In this classification, Norovirus serological reagents are devices used in test to identify specific Norovirus antibodies in serum. US FDA regulates Norovirus serological reagents under 21 CFR 866.3395 and under FDA product code OUC.

In this classification, a Nuclear matrix protein 22 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Nuclear matrix protein 22 based tumors.

Automated sample preparation systems for nucleic acid extraction, isolation and purification, resulting in purified products to be utilized in diverse nucleic acid detection systems

Replacement parts and accessories utilized on nucleic acid extraction, isolation and purification analyzers

Reagent and kit utilized for nucleic acid extraction, isolation and purification on automated systems

Isolates single cells from cell suspensions without magnetic forces

In this classification, this entry connotes an extract made of Oak used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Oat used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Oat grass used in an Immunological Allergenic test.

In this classification, Occult blood test connotes a device used to detect occult blood in urine or feces. Occult blood is blood present in such small quantities that it can be detected only by chemical tests of suspected material, or by microscopic or spectroscopic examination. US FDA regulates Occult blood test under 21 CFR 864.6550 and under FDA product code OOX.

A tester that measures the changes in condition following the temperature decline of crude petroleum and gasoline products.

A tester that tests the degree of oil film formulation for machine lubrication oil and grease types, the change of grease thickness following the temperature change and others.

A tester that is designed to test the capability of the filter that filters the impure substance within the lubricant oil used in machine by using the particle counter.

A tester that is designed to measure the volume of bubble generation that is produced by the influence of the surface tension at the time of entering into the lubrication oil for air.

A type of experiment device for laboratory that seeks the applicable dilute magnification by diluting until no more sense of odor.

In this classification, this entry connotes an extract made of Olive used in an Immunological Allergenic test.

In this classification, a Oncoproteins tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Oncoproteins based tumors.

Equipment that is used for hydraulic experiment by using the artificial waterway. It is the device used to measure the flow velocity, flow velocity distribution, river bed change, flow rate and others at the open channel with water flowing.

In this classification, a Opiate test system is a device intended to measure Opiate for clinical toxicology purposes. US FDA regulates Opiate test system under 21 CFR 862.3650 and under FDA product code DJG

Apparatus for measuring the flow rate of gas, and other flowing materials with the help of an optical laser base probe.

An optical instrument designed to ascertain the height difference or equality between two points.

Equipment that measures the change volume of finite angle by using the light reflection of mirror.

A combined power meter with 6 wavelength laser source, for optical fiber network installation and maintenance. With the large capacity of data storage, USB interface and PC software, it's very convenient for field and laboratory testing.Auto wavelength recognition,Automatically data storage.

A meter that is designed to measure the presence of the line or more in optical line work and maintenance and repairing work. It is the optical communication meter that measures the optical output coming from the optical fiber by using the light receiving sensor.

A type of device that can be used to determine the basic line in surveying or used in the precise semiconductor equipment by using the interference difference of prism arranged inside.

A type of research and experiment meter that is designed to review the change in optical wavelength, temperature, and various reliabilities of various optical devices.

A type of device that includes the light source or heat source and optical system. It is manufactured to assist the arrangement of the optical system of the infrared ray equipment.

In this classification, this entry connotes an extract made of Orange used in an Immunological Allergenic test.

In this classification, this entry connotes a standardized formulation of Organic carbon used to conduct Anion tests.

In this classification, Ornithine carbamyl transferase test system connotes a device used to measure Ornithine carbamyl transferase levels. US FDA regulates Ornithine carbamyl transferase test system under 21 CFR 862.1535 and under FDA product code JMY.

A tester that is designed to test the capability and characteristics of oscillator used to generate the voltage or current with the arbitrary frequency.

In this classification, Osmolality test system connotes a device used to measure Osmolality levels. US FDA regulates Osmolality test system under 21 CFR 862.1540 and under FDA product code JMZ.

A device for measuring osmotic pressure. Accessories include products such as sample tubes, stirring wires, sample tips.

In this classification an osmometer for clinical use is a device intended to measure the osmotic pressure of body fluids. Osmotic pressure is the pressure required to prevent the passage of a solution with a lesser solute concentration into a solution with greater solute concentration when the two solutions are separated by a semipermeable membrane. The concentration of a solution affects its osmotic pressure, freezing point, and other physiochemical properties. Osmometers determine osmotic pressure by methods such as the measurement of the freezing point US FDA regulates Osmometer for clinical use under 21 CFR 862.2730 and under FDA product code JJM.

In this classification, Osmotic fragility test connotes a device used to determine the resistance of red blood cells to hemolysis (destruction) in varying concentrations of hypotonic saline solutions. US FDA regulates Osmotic fragility test under 21 CFR 864.6600 and under FDA product code GKE.

In this classification, (OTC) Over-the-counter test sample collection systems for drugs of abuse testing are restricted devices used for sample testing that shall be performed in a laboratory using screening tests that have been approved, cleared, or otherwise recognized by the Food and Drug Administration as accurate and reliable for the testing of such specimens for identifying drugs of abuse or their metabolites US FDA regulates Otc test sample collection systems for drugs of abuse testing under 21 CFR 864.3260 and under FDA product code MPQ.

In this classification, this entry connotes a Other enzymes enzyme that is used in clinical chemistry testing.

In this classification, Ouchterlony agar plate connotes a device containing an agar gel used to examine antigen-antibody reactions. In immunodiffusion, antibodies and antigens migrate toward each other through gel which originally contained neither of these reagents. As the reagents come in contact with each other, they combine to form a precipitate that is trapped in the gel matrix and is immobilized. US FDA regulates Ouchterlony agar plate under 21 CFR 866.4600 and under FDA product code JZP.

In this classification, a Ovarian adnexal mass assessment score test system tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Ovarian adnexal mass based tumors. US FDA regulates Ovarian adnexal mass assessment score test system under 21 CFR 866.6050 and under FDA product code ONX.

In this classification, this entry connotes a substrate made of Oxalate that is used in clinical chemistry testing.

In this classification, Oxalate test system connotes a device used to measure Oxalate levels. US FDA regulates Oxalate test system under 21 CFR 862.1542 and under FDA product code LPW.

In this classification, a Oxidase screening test for gonorrhea connotes an in vitro device that consists of the articles intended to identify by chemical reaction, cytochrome oxidase, an oxidizing enzyme that is associated with certain bacteria including Neisseria gonorrhoeae. Because it is unlikely that cytochrome oxidase-positive organisms other than Neisseria gonorrhoeae are present in the urethral discharge of males, the identification of cytochrome oxidase with this device indicates presumptive infection of the patient with the causative agent of gonorrhea. US FDA regulates Oxidase screening test for gonorrhea under 21 CFR 866.2420 and under FDA product code LGA.

A tester that measures the ratio of oxidation-reduction of soluble substances within the solution.

A space that is structured with the device to generate ozone and experiment thereof in order to undertake experiment on the influence of ozone on the ecology and the degradation properties of product due to the ozone.

In this classification, a P53 tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques P53 based tumors.

Red blood haemoglobin cell concentrate

Test equipment that tests the formation of the film membrane by dipping the specimen in the paint liquid solution when coating on the paints and taking it out after certain period of time.

A tester that is designed to measure or test the hiding power of resin or paint. The hiding power is generally the capability to conceal the top coating paint or pigment, print ink, or resin applied just prior to the application.

An instrument that is designed to measure the particle size and dispensability of various paints, such as paint, print ink and others.

In this classification, this entry connotes an extract made of Palm used in an Immunological Allergenic test.

An electric instruction meter that is attached to the distribution board, cabinet panel, operation panel and others.

A tester that measures the degree of paper or fiber to absorb water.

A type of paper manufacturing device for test that is purported to undertake the characteristic test of pulp.

Electronic large volume capacity container that melts, maintains constant temperature and consistency, and dispenses liquidized histology paraffin into the tissue embedding cassette

In this classification, Parainfluenza virus serological reagents are devices used in test to identify specific Parainfluenza virus antibodies in serum. US FDA regulates Parainfluenza virus serological reagents under 21 CFR 866.3400 and under FDA product code GQP.

In this classification, Parathyroid hormone test system connotes a device used to measure Parathyroid hormone levels. US FDA regulates Parathyroid hormone test system under 21 CFR 862.1545 and under FDA product code CEW.

In this classification a partial thromboplastin time test is a device used for primary screening for coagulation abnormalities, for evaluation of the effect of therapy on procoagulant disorders, and as an assay for coagulation factor deficiencies of the intrinsic coagulation pathway US FDA regulates Partial thromboplastin time tests under 21 CFR 864.7925 and under FDA product code GFO.

A device used to generate kinetic energy by accelerating charged particles such as electrons and protons in a strong electronic field or magnetic field.It is used to analyze the deep structure of an atomic nucleus or an elementary particle.

A counter that measures the number of particles for extremely finite pulverulent body or makes comparative measurement that are found in liquid, such as working oil, ultra pure water and others.

Automated analyzer for fluid pariticle enumeration and size distribution analysis

Replacement parts, accessories and supplies for automated fluid particle enumeration and size distribution analysis

All quality controls and calibrators and standards utilized in automated particle enumeration and size distribution counters

All reagents utilized for automated fluid particle enumeration and size distribution analysis

Container for the organization and dispensing of pasteur and transfer pipettes at the workbench

In this classification, this entry connotes an extract made of Pea used in an Immunological Allergenic test.

In this classification, this commodity indicates a product used as a small cylinder that can be coated with bacteria as part of scientific experiments with antibiotics in a medical setting Most nations, for tariff and trade purposes, schedule these products under HS 901920.

In this classification, this entry connotes an extract made of Pepper used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Pepper tree used in an Immunological Allergenic test.

In this classification, this entry connotes a Pepsin enzyme that is used in clinical chemistry testing.

Equipment that synthesizes the desired peptide by controlling the amino acid required for reaction and synthesis manually or in computer by the user as the peptide made by the condensation polymerization reaction of the amino acid.

In this classification, this entry connotes an extract made of Perch used in an Immunological Allergenic test.

In this classification, this entry connotes a standardized formulation of Perchlorate used to conduct Anion tests.

An optical device that is made to see outside from the area blocked with its view, such as bunker or basement, by using the prism or mirror.

A special microscope that is made for clear observation of the interior structure for the colorless sample.

A tester that determines the phase sequence of generated voltage when the 3-phase generator is rotating to the regular rotation direction.

A type of device that changes and appropriately adjusts the hydrogen ion concentration.

In this classification, a Phenobarbital test system is a device intended to measure Phenobarbital for clinical toxicology purposes. US FDA regulates Phenobarbital test system under 21 CFR 862.3660 and under FDA product code LGQ

In this classification, this entry connotes a standardized formulation of Phenol used to conduct Anion tests.

In this classification, a Phenothiazine test system is a device intended to measure Phenothiazine for clinical toxicology purposes. US FDA regulates Phenothiazine test system under 21 CFR 862.3670 and under FDA product code DJQ

In this classification, Phenylalanine test system connotes a device used to measure Phenylalanine levels. US FDA regulates Phenylalanine test system under 21 CFR 862.1555 and under FDA product code JNB.

In this classification, this entry connotes a titrant of Phenylarsine oxide used as a reagent in clinical chemistry testing.

In this classification, this entry connotes a substrate made of Phenylketonuria that is used in clinical chemistry testing.

Container and rack used for the organization and dispensing of ancillary items such as gauze, tourniquets, needles, bandages, and lancets in the phlebotomy area

Quality controls and calibrator and standard utilized on ph meters and conductivity meters for electrochemical testing

In this classification, this entry connotes a standardized formulation of Phosphate-silica used to conduct Anion tests.

In this classification, this entry connotes a standardized formulation of Phosphate used to conduct Anion tests.

In this classification, this entry connotes a Phospho hexose isomerase enzyme that is used in clinical chemistry testing.

In this classification, Phosphohexose isomerase test system connotes a device used to measure Phosphohexose isomerase levels. US FDA regulates Phosphohexose isomerase test system under 21 CFR 862.1570 and under FDA product code JNE.

In this classification, this entry connotes a substrate made of Phospholipids that is used in clinical chemistry testing.

In this classification, Phospholipid test system connotes a device used to measure Phospholipid levels. US FDA regulates Phospholipid test system under 21 CFR 862.1575 and under FDA product code JNT.

In this classification, Phosphorus (inorganic) test system connotes a device used to measure Phosphorus (inorganic) levels. US FDA regulates Phosphorus (inorganic) test system under 21 CFR 862.1580 and under FDA product code CEO.

In this classification, this entry connotes a standardized formulation of Phosphorus used to conduct Anion tests.

Equipment that is designed to measure the strength of electric current generated from the photoelectric effect with the electrons released when the light is shed on a substance.

An instrument that measures the strength of electromagnetic radiation in the range from ultraviolet to infrared and including the visible spectrum. Most photometers convert light into an electric current using a photoresistor, photodiode, or photomultiplier.

Instrument and accessories used to measure the light intensity

An instrument that is used to measure the number of photon, one of the elementary particles.

Photosynthesis reaction is the reaction that synthesizes the carbohydrate with the energy source of carbon gas, water and inorganic chlorine from the green plant and the solar ray and with the catalyst of chlorophyll. And the device measuring it is referred to as the photosynthesis measurement apparatus.

A type of device that surveys the impact of various environment conditions on the plants. It is done by artificially building up the environment, such as temperature, humidity, light and others required of plant growth for experiment when undertaking the growth experiment of various plants.

In this classification, this entry connotes an extract made of Pigweed used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Pine used in an Immunological Allergenic test.

A measurement gauge that is used to determine the accurate angle of the workpiece.

Equipment that finds out the speed of search vessel and water temperature. When there is an accident of drowning in deep lake, river or ocean, under the poor situation with terrible water view, the scanning sonar is used to find out the location of sunken ship, floor condition, vehicle or drowned person.

A device that detects and warns the occurrence of defective pin hole on the insulation film and others coated to prevent the corrosion of the metal surface.

Paddle, tape or device utilized for perianal sampling to detect enteric pinworms

Protective canister or box used for storage of serological, volumetric, transfer and pasteur pipettes to prevent breakage

In this classification a pipetting and diluting system for clinical use is a device intended to provide an accurately measured volume of liquid at a specified temperature for use in certain test procedures. This generic type of device system includes serial, manual, automated, and semi-automated dilutors, pipettors, dispensers, and pipetting stations US FDA regulates Pipetting and diluting system for clinical use under 21 CFR 862.2750 and under FDA product code JQW.

Automated system for the calibration and volume delivery verification of manual and electronic pipettors

Replacement parts, accessories and supplies for pipettor calibration and delivery verification analyzers

Reagent or kit utilized for automated pipettor calibration and volumetric delivery verification

Reagent or kit utilized for manual pipettor calibration and volumetric delivery verification

Reservoir or boat utilized to contain reagents, solutions or stains that will be pipetted by multichannel pipettors

Measuring equipment which is designed to measure the discharge water volume in the fire extinguishing facilities, such as indoor and outdoor fire hydrants and others.

An instrument that is used for testing the ship with the compulsory motion in order to experimentally seek the hydrodynamic forces coefficients from the ship model towing tank.

In this classification, this entry connotes an extract made of Planetree used in an Immunological Allergenic test.

A type of device that is designed to measure the width of surrounded part with irregular curves on the plane.

In this classification, this entry connotes an extract made of Plantain used in an Immunological Allergenic test.

A portable tool that is used in gathering plants. The plant collection set is consisted of collection container, plant press, trowel, and pruning shears.

A type of device that measures the nurturing condition of plant periodically during certain period.

It is a device that measures the pressure that the roots of plants absorb from the soil and pushes them through the water tube to the stems or leaves. It is used to study the growth of plants.

Cryopoor plasma, Factors 8, 9,

In this classification a plasma oncometer for clinical use is a device intended to measure plasma oncotic pressure, which is that portion of the total plasma osmotic pressure contributed by protein and other molecules too large to pass through a specified semipermeable membrane. Because variations in plasma oncotic pressure are indications of certain disorders, measurements of the variations are useful in the diagnosis and treatment of these disorders US FDA regulates Plasma oncometer for clinical use under 21 CFR 862.2720 and under FDA product code JJK.

In this classification, Plasma oncometry test system connotes a device used to measure Plasma oncometry levels. US FDA regulates Plasma oncometry test system under 21 CFR 862.1530 and under FDA product code JNX.

In this classification Aaplasma viscometer for clinical use is a device intended to measure the viscosity of plasma by determining the time period required for the plasma to flow a measured distance through a calibrated glass tube. Measurements obtained by this device are used to monitor changes in the amount of solids present in plasma in various disorders US FDA regulates Plasma viscometer for clinical use under 21 CFR 862.2920 and under FDA product code JJL.

In this classification, a Plasminogen immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Plasminogen. US FDA regulates Plasminogen immunological test system under 21 CFR 866.5715 and under FDA product code DDX.

In this classification, Plasmodium species antigen detection assays are devices used in test to identify specific Plasmodium species antigen detection assays antibodies in serum. US FDA regulates Plasmodium species antigen detection assays under 21 CFR 866.3402 and under FDA product code OAX.

A tester that measures the plasticity of uncombined raw material, combined raw material, and reproduced raw material of un-vulcanized rubber and rubber substance.

A soil testing device that measures the soil settlement following the compression load in order to find out the bearing capacity of soil from road, run way and others.

In this classification, Platelet adhesion test connotes a device used to determine in vitro platelet function. US FDA regulates Platelet adhesion test under 21 CFR 864.6650 and under FDA product code JBZ.

In this classification, Platelet aggregometer connotes a device used to determine changes in platelet shape and platelet aggregation following the addition of an aggregating reagent to a platelet rich plasma. US FDA regulates Platelet aggregometer under 21 CFR 864.6675 and under FDA product code JBX.

In this classification a platelet factor 4 radioimmunoassay is a device used to measure the level of platelet factor 4, a protein released during platelet activation by radioimmunoassay. This device measures platelet activiation, which may indicate a coagulation disorder, such as myocardial infarction or coronary artery disease US FDA regulates Platelet factor 4 radioimmunoassay under 21 CFR 864.7695 and under FDA product code LCO.

Agitating incubators for platelet storage

In this classification, this entry connotes a colorimetric standard that incorporates the Platinum-cobalt Color Index.

An apparatus that brings the measuring point of the ground and the measuring point of the flat table to be on the same vertical line by using at the time of surveying.

In this classification, this entry connotes an extract made of Poison ivy used in an Immunological Allergenic test.

In this classification, Poliovirus serological reagents are devices used in test to identify specific Poliovirus antibodies in serum. US FDA regulates Poliovirus serological reagents under 21 CFR 866.3405 and under FDA product code GOH.

A space that the facilities are equipped to make various polluted environment in order to measure the impact of pollution on animal and plant, service life and other characteristics of various machines and equipments.

Designed for the sensitive, reproducible, endpoint detection and analysis of RNA molecules by RT–PCR. Using this convenient one-step formulation, you can perform both cDNA synthesis and PCR amplification in a single tube using gene-specific primers, and target RNAs from either total RNA or mRNA. The system uses a mixture of SuperScript™ III Reverse Transcriptase and Platinum™ Taq DNA Polymerase in an optimized reaction buffer, and it can detect a wide range of RNA targets, from 200 bp to 4.5 kb. The amount of starting material can range from 0.01 pg to 1 μg of total RNA.

Cool packs designing for the uniform cooling of PCR plates, tubes or strips during preparation

A type of device that is designed to test the change of pressure, volume and temperature influenced when the polymer is injected for molding.

In this classification, this entry connotes an extract made of Poplar used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Populus alba used in an Immunological Allergenic test.

In this classification, this entry connotes a substrate made of Porphobilinogen that is used in clinical chemistry testing.

In this classification, Porphobilinogen test system connotes a device used to measure Porphobilinogen levels. US FDA regulates Porphobilinogen test system under 21 CFR 862.1590 and under FDA product code JNF.

In this classification, Porphyrins test system connotes a device used to measure Porphyrins levels. US FDA regulates Porphyrins test system under 21 CFR 862.1595 and under FDA product code JKJ.

Pipettor operating on a positive displacement principle, which contains a reservoir tip, allowing for variable volume repeating dispensing from the reservoir and not from the primary sample

In this classification, this entry connotes a titrant of Potassium hydroxide used as a reagent in clinical chemistry testing.

In this classification, this entry connotes a titrant of Potassium permanganate used as a reagent in clinical chemistry testing.

In this classification, Potassium test system connotes a device used to measure Potassium levels. US FDA regulates Potassium test system under 21 CFR 862.1600 and under FDA product code MZV.

In this classification, this entry connotes an extract made of Potato used in an Immunological Allergenic test.

In this classification, potentiating media for in vitro diagnostic use are media, such as bovine albumin, that are used to suspend red cells and to enhance cell reactions for antigen-antibody testing. US FDA regulates Potentiating media for in vitro diagnostic use under 21 CFR 864.96 and under FDA product code KSG.

In this classification, this entry connotes an extract made of Povertyweed used in an Immunological Allergenic test.

A meter that is designed to measure the ratio of actual electric power and the apparent power in the electric circuit.

In this classification, a Prealbumin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Prealbumin. US FDA regulates Prealbumin immunological test system under 21 CFR 866.5060 and under FDA product code DDF.

In this classification, Pregnanediol test system connotes a device used to measure Pregnanediol levels. US FDA regulates Pregnanediol test system under 21 CFR 862.1605 and under FDA product code JLP.

In this classification, Pregnanetriol test system connotes a device used to measure Pregnanetriol levels. US FDA regulates Pregnanetriol test system under 21 CFR 862.16100 and under FDA product code JLR.

In this classification, Pregnenolone test system connotes a device used to measure Pregnenolone levels. US FDA regulates Pregnenolone test system under 21 CFR 862.1615 and under FDA product code JNG.

A meter which measures the altitude by using the pressure difference of atmosphere.

A type of device that is designed to test the capability of device that measures pressure and the normal operation thereof.

Equipment that is used when the pressure is lowered to make the pressure condition fit to the experiment.

An instrument used to measure pressure.

A transducer which is designed to detect pressure and produce an electrical signal based on the detected pressure

A commercial scale that displays the charge following the weight of the goods. There are container removing function, price computation function, and change calculation function. It is structured for measurement plate and display part.

Primary and secondary antibodies that are are available for universal detection by multiple methodologies including but not limited to fluorescent microscopy, western blot, immunopreciptiation, chromatin immunoprecipitation, flow cytometry, immunohistochemistry, immunocytochemistry, and electron microscopy

In this classification, a Primidone test system is a device intended to measure Primidone for clinical toxicology purposes. US FDA regulates Primidone test system under 21 CFR 862.3680 and under FDA product code DJD

In this classification, a processing system for frozen blood is a device used to glycerolize red blood cells prior to freezing to minimize hemolysis (disruption of the red cell membrane accompanied by the release of hemoglobin) due to freezing and thawing of red blood cells and to deglycerolize and wash thawed cells for subsequent reinfusion. US FDA regulates Processing system for frozen blood under 21 CFR 864.9145 and under FDA product code KSW.

In this classification, a Pro-gastrin-releasing peptide tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Pro-gastrin-releasing peptide based tumors.

In this classification, a Progesterone receptor assays tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Progesterone receptor assays based tumors.

In this classification, Progesterone test system connotes a device used to measure Progesterone levels. US FDA regulates Progesterone test system under 21 CFR 862.1620 and under FDA product code JLS.

In this classification, Prolactin (lactogen) test system connotes a device used to measure Prolactin (lactogen) levels. US FDA regulates Prolactin (lactogen) test system under 21 CFR 862.1625 and under FDA product code CFS.

In this classification, a Properdin factor b immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Properdin factor b. US FDA regulates Properdin factor b immunological test system under 21 CFR 866.5320 and under FDA product code JZH.

In this classification, a Propoxyphene test system is a device intended to measure Propoxyphene for clinical toxicology purposes. US FDA regulates Propoxyphene test system under 21 CFR 862.3700 and under FDA product code JXN

In this classification, Protein-bound iodine test system connotes a device used to measure Protein-bound iodine levels. US FDA regulates Protein-bound iodine test system under 21 CFR 862.1640 and under FDA product code JIK.

In this classification, this entry connotes a substrate made of Protein electrophoresis that is used in clinical chemistry testing.

In this classification, Protein (fractionation) test system connotes a device used to measure Protein (fractionation) levels. US FDA regulates Protein (fractionation) test system under 21 CFR 862.1630 and under FDA product code JQJ.

Stains specific to visualization of proteins separated by agarose gel electrophoresis, that are not polyacrylimide in composition

In this classification, a Protein s-100 b tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Protein s-100 b based tumors.

In this classification, Proteus genus (weil-felix) serological reagents are devices used in test to identify specific Proteus genus (weil-felix) antibodies in serum. US FDA regulates Proteus genus (weil-felix) serological reagents under 21 CFR 866.3410 and under FDA product code GSZ.

In this classification a prothrombin consumption tests is a device that measures the patient's capacity to generate thromboplastin in the coagulation process. The test also is an indirect indicator of qualitative or quantitative platelet abnormalities US FDA regulates Prothrombin consumption test under 21 CFR 864.7720 and under FDA product code MIF.

In this classification, a Prothrombin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Prothrombin. US FDA regulates Prothrombin immunological test system under 21 CFR 866.5735 and under FDA product code DDF.

In this classification a prothrombin-proconvertin test and thrombotest are devices used in the regulation of coumarin therapy (administration of a coumarin anticoagulant such as sodium warfarin in the treatment of venous thrombosis and pulmonary embolism) and as a diagnostic test in conjunction with, or in place of, the Quick prothrombin time test to detect coagulation disorders US FDA regulates Prothrombin-proconvertin test and thrombotest under 21 CFR 864.7735 and under FDA product code JPF.

In this classification a prothrombin time test is a device used as a general screening procedure for the detection of possible clotting factor deficiencies in the extrinsic coagulation pathway, which involves the reaction between coagulation factors III and VII, and to monitor patients receiving coumarin therapy (the administration of one of the coumarin anticoagulants in the treatment of venous thrombosis or pulmonary embolism) US FDA regulates Prothrombin time test under 21 CFR 864.7750 and under FDA product code GJS.

A standard device used for the calibration test of tension and compression load of all-purpose material tester. It is designed to use for load inspection and ordinary management of the material tester.

In this classification, Pseudomonas genus serological reagents are devices used in test to identify specific Pseudomonas genus antibodies in serum. US FDA regulates Pseudomonas genus serological reagents under 21 CFR 866.3415 and under FDA product code GSR.

An instrument that provides a visual indication of the audible effects of disturbing voltages of various frequencies

A meter that is indicated to display the period occurring with the drastic changes in voltage for the scale as operated by the current flowing in connection with the circuit.

Equipment that inspects the pump efficiency. It uses the thermal dynamics method and flux to measure.

A type of device that corrects the error of the optical pyrometer and calibrates for accurate measurement. Optical pyrometer is the device to measure the temperature by comparing the brightness of high temperature object and brightness of standard lamp.

In this classification, this entry connotes a substrate made of Pyruvate that is used in clinical chemistry testing.

In this classification, Pyruvate kinase test system connotes a device used to measure Pyruvate kinase levels. US FDA regulates Pyruvate kinase test system under 21 CFR 862.1650 and under FDA product code JNJ.

In this classification, Pyruvic acid test system connotes a device used to measure Pyruvic acid levels. US FDA regulates Pyruvic acid test system under 21 CFR 862.1655 and under FDA product code JLT.

In this classification, this entry connotes an extract made of Quack used in an Immunological Allergenic test.

In this classification, this entry connotes a reagent made of Qualitative albumin detection used in clinical chemistry testing.

In this classification, a quality control kit for blood banking reagents is a device that consists of sera, cells, buffers, and antibodies used to determine the specificity, potency, and reactivity of the cells and reagents used for blood banking. US FDA regulates Quality control kit for blood banking reagents under 21 CFR 864.9650 and under FDA product code KSF.

In this classification, a Quality control kit for culture media connotes a device that consists of paper discs (or other suitable materials), each impregnated with a specified, freeze-dried, viable microorganism, intended for medical purposes to determine if a given culture medium is able to support the growth of that microorganism US FDA regulates Quality control kit for culture media under 21 CFR 866.2480 and under FDA product code JTR.

In this classification, Quality control material (assayed and unassayed) connotes a device used to measure Quality control material (assayed and unassayed) levels. US FDA regulates Quality control material (assayed and unassayed) under 21 CFR 862.1660 and under FDA product code JJY.

In this classification, a Quality control material for cystic fibrosis nucleic acid assays is a device that consists of the reagents used to identify by immunochemical techniques Quality control material for cystic fibrosis nucleic acid assays. US FDA regulates Quality control material for cystic fibrosis nucleic acid assays under 21 CFR 866.5910 and under FDA product code NZB.

Filtration kit for SPE that facilitates extraction and clean-up of pesticide from complex matrices.

In this classification, a Quinine test system is a device intended to measure Quinine for clinical toxicology purposes. US FDA regulates Quinine test system under 21 CFR 862.3750 and under FDA product code LAL

In this classification, this entry connotes an extract made of rabbit epithelium used in an Immunological Allergenic test.

In this classification, Rabiesvirus immunofluorescent reagents are devices used in test to identify specific Rabiesvirus immunofluorescent reagents antibodies in serum. US FDA regulates Rabiesvirus immunofluorescent reagents under 21 CFR 866.3460 and under FDA product code GOI.

In this classification, Radial immunodiffusion plate connotes a device used to that consists of a plastic plate to which agar gel containing antiserum is added. In radial immunodiffusion, antigens migrate through gel which originally contains specific antibodies. As the reagents come in contact with each other, they combine to form a precipitate that is trapped in the gel matrix and immobilized. US FDA regulates Radial immunodiffusion plate under 21 CFR 866.4800 and under FDA product code JZQ.

Equipment that observes the meteorology on the upper layer. By applying the technology that combined the electromagnetic wave and sound wave technology, this meteorological instrument measures the vertical distribution of temperature, humidity, wind velocity, wind direction and others in the upper atmosphere.

In this classification, a Radioallergosorbent (rast) immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Radioallergosorbent (rast). US FDA regulates Radioallergosorbent (rast) immunological test system under 21 CFR 866.5750 and under FDA product code DHB.

A device that launches the electric wave necessary for measuring the directions for ship or aircraft in navigation and any aircraft or ship may receive the electric wave to measure the direction on the point.

A buoy of wireless transmitter that launches the electric wave to inform the location which is also referred to as the buoy type radiotelegraph.

A tester that tests the electric facilities that sends or receives radiotelegraphy, wireless phone and other electric wave.

Radioactive nuclide, chemical or cocktail utilized for radiometric detection in research applications

Equipment that analyzes the type and strength of isotope in the sample by measuring the unique released energy of the radiation isotope.

Equipment that is designed to measure the electric wave state of dense call area or call flaw area in a way of measuring the strength of signal, degree of interference, re-use of channel, degree of call volume and noise and others.

A gauge that measures the rounding part of automobile or machine component.

In this classification, this entry connotes an extract made of Ragweed used in an Immunological Allergenic test.

Equipment that is designed to measure the abrasion condition of the rail installed in order to improve the convenience and secure the safety as a part of management inspection for running rail.

An instrument that measures the maximum downthrow volume of the running rail with the dynamic load conveyed from the train when it passes the train.

A gauge that is used to measure the gap between the rail routes.

A type of device that is designed to measure the rail temperature and the gap of joint parts at the time of having the interval to the joint of rail. It occurs when the running rail is expanded and contracted in length direction in accordance with the temperature changes. It may deform 2-way direction or 1-way direction depending on each case.

An instrument that is designed to measure the external force acting on the upper part of the railroad ties when the train passes by. The running rail is installed on the upper part of the railroad tie and is joined with the spike, bolt, nut and others for its fixation.

Equipment that is used to determine the accuracy of rain gauge by supplying the water from the drop speed ranged from 20mm per hour to 30mm per hour by using the burette or rotary pump.

In this classification, this entry connotes an extract made of Raspberry used in an Immunological Allergenic test.

In this classification, Reagents for detection of specific novel influenza a viruses are devices used in test to identify specific Reagents for detection of specific novel influenza a viruses antibodies in serum. US FDA regulates Reagents for detection of specific novel influenza a viruses under 21 CFR 866.3332 and under FDA product code NXD.

In this classification a red blood cell enzyme assay is a device used to measure the activity in red blood cells of clinically important enzymatic reactions and their products, such as pyruvate kinase or 2,3-diphosphoglycerate US FDA regulates Red blood cell enzyme assay under 21 CFR 864.7100 and under FDA product code LKZ.

In this classification, a red cell indices device, usually part of a larger system, calculates or directly measures the erythrocyte mean corpuscular volume (MCV), the mean corpuscular hemoglobin (MCH), and the mean corpuscular hemoglobin concentration (MCHC). US FDA regulates Red cell indices device under 21 CFR 864.5300 and under FDA product code KQH.

In this classification a red cell lysing reagent is a device used to lyse (destroy) red blood cells for hemoglobin determinations or aid in the counting of white blood cells US FDA regulates Red cell lysing reagent under 21 CFR 864.8540 and under FDA product code GGK.

In this classification a refractometer for clinical use is a device intended to determine the amount of solute in a solution by measuring the index of refraction (the ratio of the velocity of light in a vacuum to the velocity of light in the solution). The index of refraction is used to measure the concentration of certain analytes (solutes), such a plasma total proteins and urinary total solids.  US FDA regulates Refractometer for clinical use under 21 CFR 862.2800 and under FDA product code JRE.

Gel and liquid refrigerant pack utilized in maintaining a refrigerated environment within a diagnostic specimen shipping container

Rack or tray used for short or long term refrigerated storage of specimens

A type of precision safety diagnosis equipment for the concrete structures that detects the iron reinforcing rod buried under the concrete structure or bridge and surveys the location and distance of the steel frames.

A tester that tests if the operation time or holding figure of relay that is controlled electrically is correctly operated to meet the standard.

Programmable wired or wireless remote or onsite monitoring system capable of multimodal transactions regarding temperature and humidity within all aspects of a laboratory environment in order to protect and validate analyzer, reagent, blood product and specimen integrity

In this classification, Reovirus serological reagents are devices used in test to identify specific Reovirus antibodies in serum. US FDA regulates Reovirus serological reagents under 21 CFR 866.3470 and under FDA product code GQB.

Reservoir style pipette "tip" that is used for pipetting with positive displacement repeating pipettors

All bedding materials utilized for the skeletal support, comfort, warmth and dryness of animals in a bioresearch laboratory

Food and diet used for the nutrition of animals in a bioresearch laboratory

Chamber or hood used for the induction of anesthesia into animals in a bioresearch laboratory

Test kit used for the purpose of measurement of biophysical and biochemical analytes in animals in a bioresearch laboratory

A wire wound and thin film device that measures temperature using the physical principle of the positive temperature coefficient of electrical resistance of metals. The hotter they become, the larger or higher the value of their electrical resistance.

Test equipment that is used for testing the characteristics of temperature, voltage and current of resistance.

In this classification, Respiratory syncytial virus serological reagents are devices used in test to identify specific Respiratory syncytial virus antibodies in serum. US FDA regulates Respiratory syncytial virus serological reagents under 21 CFR 866.3480 and under FDA product code GQF.

In this classification, this entry connotes a device used to perform a Respiratory viral panel multiplex nucleic acid assay. US FDA regulates Respiratory viral panel multiplex nucleic acid assay under 21 CFR 866.3980 and under FDA product code OCC.

A type of device that is designed to measure the discharge gases, such as carbon gas, that are released to outside of body for certain time, periodically or consecutively through the chemical change of substance within the body and building up the oxygen volume supplied from outside to sustain the plant or animal life.

In this classification, a Retinol-binding protein immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Retinol-binding protein. US FDA regulates Retinol-binding protein immunological test system under 21 CFR 866.5765 and under FDA product code CZS.

Equipment and accessories that increase the pressure of the high concentration side, it can make water pass from the high salt concentration side to the one with low concentration

In this classification, a Rheumatoid factor immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Rheumatoid factor. US FDA regulates Rheumatoid factor immunological test system under 21 CFR 866.5775 and under FDA product code DHR.

In this classification, Rhinovirus serological reagents are devices used in test to identify specific Rhinovirus antibodies in serum. US FDA regulates Rhinovirus serological reagents under 21 CFR 866.3490 and under FDA product code GQE.

It is used to evaluate the taste of rice in percentage by surveying and measuring the electromagnetic wave on the moisture protection membrane formed on the surface of the rice when actually cooked. It is also used for researches in developing the seed of rice.

In this classification, Rickettsia serological reagents are devices used in test to identify specific Rickettsia antibodies in serum. US FDA regulates Rickettsia serological reagents under 21 CFR 866.3500 and under FDA product code GPS.

A test board to confirm mechanical connections and other elements of vehicle wiring harnesses.

In this classification, Rna preanalytical systems connotes a device used to collect, store, and transport patient specimens, and stabilize intracellular RNA from the specimens, for subsequent isolation and purification of the intracellular RNA for RT-PCR used in in vitro molecular diagnostic testing. US FDA regulates Rna preanalytical systems under 21 CFR 866.4070 and under FDA product code NTW.

RNase Inhibitor inhibits the activity of RNases A,B and C by binding them in a noncompetitive mode at a 1:1 ratio. It does not inhibit eukaryotic RNases T1, T2, U1, U2, CL3 as well as prokaryotic RNases I and H. Highlights • Performs under a wide range of reaction conditions • Protects RNA from degradation at temperatures up to 55°C Note DTT provided in the Storage Buffer ensures stability during long term storage, but is not necessary for inhibitor activity. Recommended concentration 1 U/ µL of a reaction mixture. For Research Use Only. Not for use in diagnostic procedures.

Measurement equipment for road management that measures and records the flatness of paved road with asphalt and cement concrete.

In this classification, Rocket immunoelectrophoresis equipment connotes a device used to perform a specific test on proteins by using a procedure called rocket immunoelectrophoresis. In this procedure, an electric current causes the protein in solution to migrate through agar gel containing specific antisera. The protein precipitates with the antisera in a rocket-shaped pattern, giving the name to the device. The height of the peak (or the area under the peak) is proportional to the concentration of the protein. US FDA regulates Rocket immunoelectrophoresis equipment under 21 CFR 866.4830 and under FDA product code JZX.

In this classification, Rubella virus serological reagents are devices used in test to identify specific Rubella virus antibodies in serum. US FDA regulates Rubella virus serological reagents under 21 CFR 866.3510 and under FDA product code GON.

In this classification, Rubeola (measles) virus serological reagents are devices used in test to identify specific Rubeola (measles) virus antibodies in serum. US FDA regulates Rubeola (measles) virus serological reagents under 21 CFR 866.3520 and under FDA product code GRJ.

In this classification a Russell viper venom reagent is a device used to determine the cause of an increase in the prothrombin time US FDA regulates Russell viper venom reagent under 21 CFR 864.8950 and under FDA product code GIR.

A tester that tests the rust preventive capability of lubricant oil that is applied on the metal surface in the event of mixing the water or salt water on the lubricant.

In this classification, this entry connotes an extract made of Rye used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Ryegrass used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Sage used in an Immunological Allergenic test.

In this classification, a Salicylate test system is a device intended to measure Salicylate for clinical toxicology purposes. US FDA regulates Salicylate test system under 21 CFR 862.3830 and under FDA product code DKG

In this classification, Salmonella genus serological reagents are devices used in test to identify specific Salmonella genus antibodies in serum. US FDA regulates Salmonella genus serological reagents under 21 CFR 866.3550 and under FDA product code GRL.

In this classification, this entry connotes an extract made of Saltbush used in an Immunological Allergenic test.

In this classification, this entry connotes an extract made of Saltgrass used in an Immunological Allergenic test.

A type of device that is designed to manufacture the samples by to fit into the specification when the physical features in object, material or others are measured.

A tester that measures the unit weight of earth with the maximum particle radius of 5cm or less under the sand replacement method at the site.

A measurement tube that measures the volume of sand and others by installing the sensor and others to the pipe where sand and others are passed or passing the sand and others on the upper pipe to pass the lower part with the water in the glass pipe or plastic pipe with the scale.

In this classification, this entry connotes an extract made of Scale used in an Immunological Allergenic test.

Safety device utilized to remove scalpel and knife blades from handles

In this classification, Schistosoma genus serological reagents are devices used in test to identify specific Schistosoma genus antibodies in serum. US FDA regulates Schistosoma genus serological reagents under 21 CFR 866.3600 and under FDA product code GNH.

Cylindrical container with screw cap composed of glass, translucent polypropylene or opaque polyethylene used in the laboratory setting for chromatography, gamma or scintillation counting.

A gauge designed to measure the shape of a cross-recessed groove and the depth of the hole inscribed on the head of the screw components including, cross-recessed head machine screws, cross-recessed head taping screws, cross-recessed head wood screws and the like.

In this classification, this entry connotes an extract made of Sea blight used in an Immunological Allergenic test.

In this classification, a Selective culture medium connotes a device using Selective media allow certain types of organisms to grow, and inhibit the growth of other organisms. US FDA regulates Selective culture medium under 21 CFR 866.2360 and under FDA product code JSI.

Test kit used for fertility analysis.

In this classification, this entry connotes a reagent made of Semen bicarbonate-formalin diluting fluid used in clinical chemistry testing.

In this classification, a Seminal fluid (sperm) immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Seminal fluid (sperm). US FDA regulates Seminal fluid (sperm) immunological test system under 21 CFR 866.58 and under FDA product code DGB.

In this classification, a Serotonin tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Serotonin based tumors.

In this classification, Serratia genus serological reagents are devices used in test to identify specific Serratia genus antibodies in serum. US FDA regulates Serratia genus serological reagents under 21 CFR 866.3630 and under FDA product code GTA.

Tube style filter that is inserted into a blood collection tube specimen which has been centrifuged in order to separate plasma or serum from the cellular components of that blood

Equipment that tests the capability of the servo system and its auxiliary parts of auto control system with the mechanical location and angle for controlled volume.

In this classification, Shigella genus serological reagents are devices used in test to identify specific Shigella genus antibodies in serum. US FDA regulates Shigella genus serological reagents under 21 CFR 866.3660 and under FDA product code LSN.

In this classification a sickle cell test is a device used to determine the sickle cell hemoglobin content of human blood to detect sickle cell trait or sickle cell diseases US FDA regulates Sickle cell test under 21 CFR 864.7825 and under FDA product code GHM.

In this classification, this entry connotes a standardized formulation of Silica used to conduct Anion tests.

In this classification, this entry connotes a titrant of Silver nitrate used as a reagent in clinical chemistry testing.

A measurement tool that is used to find out the accurate angle of the workpiece.

In this classification, a Sirolimus test system is a device intended to measure Sirolimus for clinical toxicology purposes. US FDA regulates Sirolimus test system under 21 CFR 862.3840 and under FDA product code NRP

Equipment that examines the skin condition with the measurement of skin oil, moisture, elasticity, pores, pigment and others.

A type of device that measures the sludge, such as solid substance or floating substance contained in the liquid of water source or waste water from the plant.

A measuring instrument that precisely measures by using the method of infrared ray and others for the thickness of sludge generated from the sedimentation tank of the water supply and sewer as well as the condensation tank.

A tester that is used for concrete to measure the consistency of the concrete to make the appropriate concrete.

A tester that measures the volume of smoke generated from the process of experimenting the chemical reaction in a laboratory.

In this classification, this entry connotes a titrant of Sodium carbonate used as a reagent in clinical chemistry testing.

In this classification, this entry connotes a reagent made of Sodium citrate aqueous solution used in clinical chemistry testing.

In this classification, this entry connotes a reagent made of Sodium phosphate used in clinical chemistry testing.

In this classification, Sodium test system connotes a device used to measure Sodium levels. US FDA regulates Sodium test system under 21 CFR 862.1665 and under FDA product code JGS.

In this classification, this entry connotes a titrant of Sodium thiosulfate used as a reagent in clinical chemistry testing.

A tester that is used for evaluating the resistance for bending, a mechanical property of soft material, like the magnetic tape, film plastic, textile, and paper products.

A type of device that is designed to measure the aggregation as the physical property of soil.

A type of device that is designed to measure the chemical ingredient of lime, magnesium, potassium, fluorine, phosphorus and others contained in soil in ppm unit.

A tester that is needed for designing and constructing for dam body and drainage hole by knowing the uplift pressure on the structure installed underneath water, inundation area of base ground or dam body of earth dam, river bank, reclaimed dike.

A tester that is used to measure the liquid limit of soil.

A tester that is used for soil survey that measures the hardness of earth for finding out the road or cross section of the ground in engineering works.

A tester that measures the plastic limit of soil.

A tester that measures the contraction limit of soil. The shrinkage limit of soil has its volume not reduced even if the water content of soil is reduced to certain volume or below, and if the water content is increased this device indicates the increase of volume which is shown in function ratio of limit.

Equipment that is designed to measure accurately the soil texture for the users.

A type of device that is used to determine the compression strength and sensitivity of soil.

In order to determine the bearing capacity, the loading plate is installed above the foundation base and applies the weight to measure the settlement on each weight to find the load and subsidence curve. This is a tester that is designed to measure the permitted yield strength of the foundation from the yield strength obtained from the loading test by the loading plate.

A type of device that measures the number of somatic cells.

A buoy that has the sound detector and the wireless transmitter built-in. It is used to detect the location and confirm the location of submarine, noise under the sea, and situation of sound dispersion.

In this classification, this entry connotes a Sorbitol dehydrogenase enzyme that is used in clinical chemistry testing.

In this classification, Sorbitol dehydrogenase test system connotes a device used to measure Sorbitol dehydrogenase levels. US FDA regulates Sorbitol dehydrogenase test system under 21 CFR 862.1670 and under FDA product code JNK.

In this classification, this entry connotes an extract made of Sorghum used in an Immunological Allergenic test.

A sound detector with the stethoscope-shape that is contacted to an object to detect the abnormal sound.

Plated agarose media with nutrient ingredients favorable to the general and selective growth of yeast

An instrument that measures the specific heat as the required calorie that is required for unit weight of certain object to increase 1 degree C.

Containers used for holding specimens.

Box, usually containing a lock mechanism, which is utilized for the receipt and storage of recently collected specimens and which maintains a tamper free environment until that specimen is transported to the testing laboratory

A tester that is designed to measure the expansion height following the time lapse for 96 hours as it is dipped in water with the defined load on the earth specimen produced with the pounding on mold.

In this classification specimen transport or storage container connotes a device used in the storage or transport of various types of human or animal specimens. US FDA regulates Specimen transport and storage container under 21 CFR 864.3250 and under FDA product code KDT.

Tube used for the aliquoting of urine, plasma, serum, whole blood, cerebrospinal fluid or body fluid for the purpose of transport or storage in a tube other than the primary collection tube

A type of device that is used to measure the reflection and penetration for each wavelength of plant. It is also used to measure the amount of radiation for each wavelength of indoor artificial lights.

Accessories adding speed and a better sample identification to an autosampler

In this classification, Sporothrix schenckii serological reagents are devices used in test to identify specific Sporothrix schenckii antibodies in serum. US FDA regulates Sporothrix schenckii serological reagents under 21 CFR 866.3680 and under FDA product code GMA.

In this classification, this entry connotes an extract made of Spruce used in an Immunological Allergenic test.

In this classification, a Squamous cell carcinoma antigen tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Squamous cell carcinoma antigen based tumors.

In this classification, this entry connotes an extract made of Squash used in an Immunological Allergenic test.

In this classification, a stabilized enzyme solution is a reagent intended for medical purposes that is used to enhance the reactivity of red blood cells with certain antibodies, including antibodies that are not detectable by other techniques. These enzyme solutions include papain, bromelin, ficin, and trypsin. US FDA regulates Stabilized enzyme solution under 21 CFR 864.9400 and under FDA product code KSK.

Robotic device to handle SBS microplates.Such robots may be liquid handlers which aspirate or dispense liquid samples from and to these plates, or plate movers which transport them between instruments.

An aggregate sample that is defined for several properties to compare and test the capability and properties of aggregates.

In this classification, Staphylococcus aureus serological reagents are devices used in test to identify specific Staphylococcus aureus antibodies in serum. US FDA regulates Staphylococcus aureus serological reagents under 21 CFR 866.3700 and under FDA product code GTN.

Equipment that is designed to measure the presence of electric volume or its volume not moved that is shown on the friction object.

Units for the static concentration of clinical samples prior to analysis

A tester that is designed to measure the emulsification on the oil vapor.

A solution used to reconstitute and dilute peste des petits ruminants (PPR) vaccines.

In this classification, Streptococcus genus exoenzyme reagents are devices used in test to identify specific Streptococcus genus exoenzyme reagents antibodies in serum. US FDA regulates Streptococcus genus exoenzyme reagents under 21 CFR 866.3720 and under FDA product code GTP.

In this classification, Streptococcus genus serological reagents are devices used in test to identify specific Streptococcus genus antibodies in serum. US FDA regulates Streptococcus genus serological reagents under 21 CFR 866.3740 and under FDA product code GTY.

Equipment that tests the resistance arising from the object when it is applied with the external force (load) as the stress.

Specially designed material for use in distillation columns and chemical reactors.

In this classification, this entry connotes a standardized formulation of Sucrose used to conduct Anion tests.

In this classification, this entry connotes an extract made of Sugar used in an Immunological Allergenic test.

In this classification, this entry connotes a standardized formulation of Sulfate used to conduct Anion tests.

In this classification a sulfhemoglobin assay is a device consisting of the reagents, calibrators, controls, and instrumentation used to determine the sulfhemoglobin (a compound of sulfur and hemoglobin) content of human blood as an aid in the diagnosis of sulfhemoglobinemia (presence of sulfhemoglobin in the blood due to drug administration or exposure to a poison). This measurement may be made using methods such as spectroscopy, colorimetry, spectrophotometry, or gasometry US FDA regulates Sulfhemoglobin assay under 21 CFR 864.7490 and under FDA product code GKA.

In this classification, a Sulfonamide test system is a device intended to measure Sulfonamide for clinical toxicology purposes. US FDA regulates Sulfonamide test system under 21 CFR 862.3850 and under FDA product code DKW

In this classification, this entry connotes an extract made of Sumac used in an Immunological Allergenic test.

An analysis device that is designed for separation and determination of the compounds by using the supercritical fluid as mobile phase.

A sensor used in the coil assembly of supplemental inflator restraint SIR or air bag systems to confirm presence of necessary components.

In this classification, a Supplement for culture media connotes a device used for  customizing the growth conditions of your cells, improving cell viability and growth, and keeping cells healthier longer. US FDA regulates Supplement for culture media under 21 CFR 866.2450 and under FDA product code JSK.

In this classification, Support gel connotes a device that consists of an agar or agarose preparation that is used while measuring various kinds of, or parts of, protein molecules by various immunochemical techniques, such as immunoelectrophoresis, immunodiffusion, or chromatography. US FDA regulates Support gel under 21 CFR 866.4900 and under FDA product code JZR.

A thin plate that is used for surveying. It is used to move the principal point and each direction line by securing on the photo.

A tester that is designed to measure the solid substance found in several liquids and semi-liquid substances.

Automated system for collection and testing of sweat chloride by iontohporesis methodology for cystic fibrosis screening

Replacement parts and accessories utilized for iontophoretic sweat chloride collection and automated testing systems

A tester that is designed to test durability following the switch motion of various switches or plugs and receptacles.

In this classification, this entry connotes an extract made of Sycamore used in an Immunological Allergenic test.

In this classification, synthetic cell and tissue culture media and components are substances that are composed entirely of defined components (e.g., amino acids, vitamins, inorganic salts) that are essential for the survival and development of cell lines of humans and other animals. US FDA regulates Synthetic cell and tissue culture media and components under 21 CFR 864.2220 and under FDA product code KIT.

In this classification, a Systemic lupus erythematosus immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Systemic lupus erythematosus. US FDA regulates Systemic lupus erythematosus immunological test system under 21 CFR 866.5820 and under FDA product code DHC.

An instrument used to measure distances and, at the same time, horizontal and vertical angles.

In this classification, Tacrolimus test system connotes a device used to measure Tacrolimus levels. US FDA regulates Tacrolimus test system under 21 CFR 862.1678 and under FDA product code MLM.

Pathology Chain of Custody protocols require locked and tamper proof storage boxes, bags and cups for evidentiary specimens.

A gauge that measures the inside diameter of pipes, various holes, and the size of taper part in the gap.

A tester that verifies the running distance of the taxi meters installed in the business or individual taxi.

A tester that measures the strength of tearing by applying certain load on textile, paper, vinyl, leather and others.

Test equipment that determines the presence of malfunctioning by testing the transmission and receiving function, bell, call sensitivity and others of the telephone as the communication terminal.

A gauge that is designed to measure the diameter or width of the hole or groove with the plunger in which the spring is loaded. When the handle screw is rotated, the plunger is accurately affixed.

A tester that tests reception function image, blanking condition, number of scanning line, and voice reception condition to determine any problem for the television.

A space that the facilities are equipped to adjust the change of temperature and humidity in order to measure the impact of change of temperature and humidity on animal and plant, service life and other characteristics of various machines and equipments. It is the equipment of large space where people may walk around.

A test chamber capable of cycling through a wide range of temperatures, typically from well below the freezing point of water to well above its boiling point.

A measurement device used to indicate the temperature of an item being monitored.

An instrument designed to detect temperature changes.

Graduated penetration depth device for performing template bleeding times and/or the blotting paper used in the testing process

A tester that applies the load until the specimen is pulled in certain speed to break down. This is to measure the tensile strength, most representative mechanical strength characteristic in various materials.

A non-destructive testing device that inspects the inside of a subject by using the electromagnetic wave characteristics of terahertz waves.

Racks and containers for the orgnaization and dispensing of test and culture tubes at the workbench

A taper gauge that is the auxiliary tool to use in the static level test that surveys the parallelism and straightness of machine tool, measuring apparatus and others and shaking on the rotating shaft.

Test kits for laboratory personnel provider performed proficiency assessment and laboratory performance improvement tracking probes in multidepartmental platforms

In this classification, Testosterone test system connotes a device used to measure Testosterone levels. US FDA regulates Testosterone test system under 21 CFR 862.1680 and under FDA product code CDZ.

A thermal processing tester that dries the sample or evaluates dimensional stability by solidifying the shape or affixing the dye mainly on the dye sample of woven fabric or knitted fabric.

A tester that measures the property to recover to the original condition for the wrinkle generated from using the textile.

A tester that is related to the textile that measures draping of textile.

A type of device that measures the maturity condition for the cotton. It displays the degree of growth by the diaphragm on the cotton textile.

Equipment that measures or tests the air permeability from the properties of textile or paper.

Equipment that measures the strength from the properties of textile or paper.

A tester that tests the phenomenon of peeling off the surface by the friction with the textile or knit.

A tester that is used when measuring the washing shrinkage rate of cotton, bast fiber fabric and kind of cotton bast fiber blend fabrics.

A tester that tests the resistance on wetting of water for water-proofed textile, fiber and paper.

In this classification, a Theophylline test system is a device intended to measure Theophylline for clinical toxicology purposes. US FDA regulates Theophylline test system under 21 CFR 862.3880 and under FDA product code KLS

A tester that is designed to measure the expansion rate of the length generally following the temperature, namely, coefficient of linear expansion.

Device that detects radiation in the infrared range of the electromagnetic spectrum.

A tester that is designed to measure the change of material from the thermal stress arising from quick heating or quick freezing.

A tester that measures the degree of maintaining the body temperature or heat transfer coefficient on the external air, namely, thermokeeping of the textile goods, such as textile for clothes, filling cotton, blanket, rug, leather and others.

A scale that is used to measure the weight of certain mass when a substance is heated or maintained for certain degree of high temperature.

A device that sends the current or voltage signal to the indicator or recorder by sensing or measuring the temperature and humidity.

Replacement part or fitting utilized on a thin layer chromatograph

A sheet of metal, glass or plastic, that is coated with a thin layer of solid silica or alumina absorbent, and is utilized for thin layer chromatographic separation of a mixture's components through capillary action

In this classification a thin-layer chromatography (TLC) system for clinical use is a device intended to separate one or more drugs or compounds from a mixture. The mixture of compounds is absorbed onto a stationary phase or thin layer of inert material (e.g., cellulose, alumina, etc.) and eluted off by a moving solvent (moving phase) until equilibrium occurs between the two phases US FDA regulates Thin-layer chromatography system for clinical use under 21 CFR 862.2270 and under FDA product code KZS.

In this classification, this entry connotes a standardized formulation of Thiocyanate used to conduct Anion tests.

In this classification, this entry connotes a titrant of Thiocyanate used as a reagent in clinical chemistry testing.

In this classification, this entry connotes a standardized formulation of Thiosulfate used to conduct Anion tests.

In this classification, this entry connotes an extract made of Thistle used in an Immunological Allergenic test.

This is used to inspect the pitch of internal or external screw.

In this classification a thrombin time test is a device used to measure fibrinogen concentration and detect fibrin or fibrinogen split products for the evaluation of bleeding disorders US FDA regulates Thrombin time test under 21 CFR 864.7875 and under FDA product code GJA.

In this classification a thromboplastin generation test is a device used to detect and identify coagulation factor deficiencies and coagulation inhibitors US FDA regulates Thromboplastin generation test under 21 CFR 864.7900 and under FDA product code GKQ.

In this classification, a Thymidine kinase tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Thymidine kinase based tumors.

In this classification, this entry connotes a substrate made of Thymol that is used in clinical chemistry testing.

In this classification, a Thyroid autoantibody immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Thyroid autoantibody. US FDA regulates Thyroid autoantibody immunological test system under 21 CFR 866.5870 and under FDA product code JZO.

In this classification, Thyroid stimulating hormone test system connotes a device used to measure Thyroid stimulating hormone levels. US FDA regulates Thyroid stimulating hormone test system under 21 CFR 862.1690 and under FDA product code JLW.

In this classification, Thyroxine-binding globulin test system connotes a device used to measure Thyroxine-binding globulin levels. US FDA regulates Thyroxine-binding globulin test system under 21 CFR 862.1685 and under FDA product code CEE.

A measurement instrument for tire thickness that is designed to measure the abrasion limit of vehicle tires under the Road Transportation Act.

A tester that tests the maneuverability and safety of the tires from the external forces.

In this classification, a Tissue associated protein tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Tissue associated protein based tumors.

Baths used specifically for the controlled thawing and incubation of tissue cultures and tissue culture media

A multiple chambered glass or plastic microscope slide used for viewing cell cultures, which possesess inert hydrophobic well borders defining the cell culture area and that can be used for different stains, treatments, or fixation processes without affecting the adjacent chambers

Drum style mixer used for tissue culture, bacterial culture and mini prep by using the roller tube method that provides continous rotary motion under a constant speed and which withstands incubation temperatures

In this classification, Tissue processing equipment connotes a device used to process human or animal tissue so it can be utilized to visualize normal and abnormal structures. US FDA regulates Tissue processing equipment under 21 CFR 864.3010 and under FDA product code KET.

In this classification, this entry connotes an extract made of Tobacco used in an Immunological Allergenic test.

In this classification, a Tobramycin test system is a device intended to measure Tobramycin for clinical toxicology purposes. US FDA regulates Tobramycin test system under 21 CFR 862.3900 and under FDA product code KLB

In this classification, this entry connotes a reagent made of Toluidine blue aqueous solution used in clinical chemistry testing.

In this classification, this entry connotes a substrate made of Total lipids that is used in clinical chemistry testing.

In this classification, this entry connotes a substrate made of Total porphyrin that is used in clinical chemistry testing.

In this classification, a Total prostatic specific antigen tumor associated antigen immunological test system that consists of the reagents used to identify by immunochemical techniques Total prostatic specific antigen based tumors.

In this classification, this entry connotes a substrate made of Total protein that is used in clinical chemistry testing.

In this classification, Total protein test system connotes a device used to measure Total protein levels. US FDA regulates Total protein test system under 21 CFR 862.1635 and under FDA product code JGP.

In this classification, a Total spinal fluid immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Total spinal fluid. US FDA regulates Total spinal fluid immunological test system under 21 CFR 866.5860 and under FDA product code DFI.

In this classification, Total thyroxine test system connotes a device used to measure Total thyroxine levels. US FDA regulates Total thyroxine test system under 21 CFR 862.1700 and under FDA product code KLI.

In this classification, Total triiodothyronine test system connotes a device used to measure Total triiodothyronine levels. US FDA regulates Total triiodothyronine test system under 21 CFR 862.1710 and under FDA product code CDP.

In this classification, Toxoplasma gondii serological reagents are devices used in test to identify specific Toxoplasma gondii antibodies in serum. US FDA regulates Toxoplasma gondii serological reagents under 21 CFR 866.3780 and under FDA product code GMN.

Measuring equipment that is used to find out the status of transmission of data when sent from the communication device.

In this classification, a Transferrin immunological test system is a device that consists of the reagents used to identify by immunochemical techniques Transferrin. US FDA regulates Transferrin immunological test system under 21 CFR 866.5880 and under FDA product code JNM.

In this classification, a transfer set is a device intended for medical purposes that consists of a piece of tubing with suitable adaptors used to transfer blood or plasma from one container to another. US FDA regulates Transfer set (blood/plasma) under 21 CFR 864.9875 and under FDA product code KSB.

A tester that is to analyze the rated voltage, rated current, function or characteristic of the transformer used in electric and electronic circuit.

A surveying instrument that is used for measuring the horizontal and vertical angles for two points. This device has the center of two same axles.

Electron transparent films or electron opaque grids utilized to support specimens when being studied by transmission electron microscopy

Box used for storage of specimen grids utilized in transmission electron microscopy