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Insulin-Like Growth Factor Binding Protein-1 Immunoassay Suppliers

 EMAIL INQUIRY to  3 suppliers  
DRG International, Inc. | Address: 1167 US Highway 22 East, Mountainside, New Jersey 07092, USA USA
www.drg-international.com | Send Inquiry | Phone: +1-(908)-233-2075
FDA Registration: 2245285  Year Established: 1970  Annual Revenues: USD 10-25 Million  Employee Count: ~100  Quality: ISO 9000, ISO 9001, CE Certified
Products: Laboratory Equipment, Incubators, Amylase, Incubator Shakers, Angiotensin II, Lyme Disease (Borrelia) Test Kits, ...
DRG International, Inc. is a multinational specialty medical equipment and diagnostics manufacturer & distributor. We offer products for enzyme immunoassays, rapid saliva & tumor tests, radio immunoas more...
 
Mediagnost Gmbh | Address: Aspenhaustr. 25, Reutlingen D-72770, Germany Germany
www.mediagnost.de | Send Inquiry | Phone: +49-(0)-7121 / 51484-0
FDA Registration: 3003283395
Products: IGF-1, Endocrinology Reagents and Testing Kit, Phospho-specific IGF-1 R ELISA Kits, Rat IGF-1 Radioimmunoassay Kit, Human IGFBP-3 ELISA Kit, IGF-BP3 Radioimmunoassay Test kits, ...
Mediagnost Gmbh develops, manufactures and distributes diagnostic products for use in research & clinical practice in the areas of endocrinology, infectious diseases and neurology. Enzyme immunoassay more...
Pro-Lab, Inc. | Address: 40 Hanlan Road - Bldg. 45,, Vaughan (Toronto),, Ontario L4L 3P6, Canada Canada
www.prolabinc.com
FDA Registration: 8010383
Products: Anaerobic Identification Kit Test (FDA Code: JSP), Escherichia Coli Antigens (FDA Code: GMZ), Escherichia Coli Antisera (FDA Code: GNA), General Nutrient Broth Culture Media (FDA Code: JSC), Gram Negative Identification Panel (FDA Code: LQM), Human/Horse/Rabbit Coagulase Plasma (FDA Code: JTL), ...
Pro-Lab, Inc. is the manufacturer of safety test kits. Our test kit provides precise measurement of specific life threatening pollutants. Our test kits include mold, radon, carbon monoxide, lead in pa more...
 EMAIL INQUIRY to  3 Insulin-Like Growth Factor Binding Protein-1 Immunoassay suppliers  
FDA Code / Regulation: OAM / 862.1550

A urinary pH (nonquantitative) test system is a device intended to estimate the pH of urine. Estimations of pH are used to evaluate the acidity or alkalinity of urine as it relates to numerous renal and metabolic disorders and in the monitoring of patients with certain diets.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 862.9.

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