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Clostridium Difficile Antigen Suppliers

 EMAIL INQUIRY to  5 suppliers  
Inverness Medical Innovations, Inc. | Address: 51 Sawyer Rd., Suite 200, Waltham, Massachusetts 02453-3448, USA USA
www.invernessmedical.com | Send Inquiry | Phone: +1-(781)-647-3900
FDA Registration: 3004011380  Year Established: 2005  Annual Revenues: USD 25-50 Million  Employee Count: ~180  Quality: CE Certified
Products: Myoglobin (FDA Code: DDR), Ovulation (Luteinizing Hormone) Test Kits, Fertility Monitors, Pregnancy Test Kits, Home pregnancy test kits, Hcg, Influenza A and B Testing rapid Influenza Testing, Automated Urinalysis System (FDA Code: KQO), ...
Inverness Medical Innovations, Inc. manufactures, markets & distributes agents for use in women's health, cardiology and infectious disease. We offer research, development and supply of professional d more...
 
Wampole Laboratories | Address: 2 Research Way, Princeton, New Jersey 08540, USA USA
www.wampolelabs.com | Phone: +1-(609)-627-8000
FDA Registration: 9710052  Year Established: 2002  Annual Revenues: USD 10-25 Million  Employee Count: ~80
Products: Lyme Disease (Borrelia) Test Kits, Mononucleosis Antibody (MONO) Test Kits, Fecal Occult Blood Test Kits, Hematocrit Analyzers, Streptococcus Test Kits, Chlamydia Test Kits, ...
Wampole Laboratories, a wholly owned subsidiary of Inverness Medical Inc., provides diagnostic testing & automation solutions for the clinical laboratory & point-of-care markets. Our full product line more...
Mardx Diagnostics, Inc. | Address: 5919 Farnsworth Ct., Carlsbad, California 92008, USA USA
Phone: +1-(760)-929-0500
FDA Registration: 2245544  Annual Revenues: USD 5-10 Million
Products: Coagulation Analyzers (FDA Code: GKP), Lyme Disease (Borrelia) Test Kits, Automated Coagulation Analyzer (FDA Code: GKP), Analyte Specific Reagents, Asr Reagents (FDA Code: MVU), Infectious Disease Test Kits, Automated Coagulation Instrument (FDA Code: GKP), ...
Mardx Diagnostics, Inc. is engaged in developing, manufacturing, and marketing of diagnostic products. We offer western blot, IFA, EIA,and ENA IgG marstripe immunostride tests for 6 extractable nuclea more...
Techlab, Inc. | Address: 2001 Kraft Drive, Blacksburg, Virginia 24060-6364, USA USA
www.techlab.com | Send Inquiry | Phone: +1-(540)-953-1664, 800-832-4522
FDA Registration: 1122855  Year Established: 1989  Annual Revenues: USD 1-5 Million  Employee Count: ~40  Quality: ISO 13485 Certified
Products: Incubators, Cotton Swabs, Rapid Immunochromatographic Tests, Clostridium Difficile Antigen (FDA Code: MCB), Enzyme Immunoassay, Lactoferrin (FDA Code: DEG), ...
Techlab, Inc. develops, manufactures, and distributes rapid non-invasive intestinal diagnostics in the areas of intestinal inflammation, antibiotic associated diarrhea and parasitology. Our services i more...
Microgen Bioproducts Ltd. | Address: 1 Admiralty Way, Camberley, Surrey GU15 3DT, United Kingdom United Kingdom
www.procurnet.com | Phone: +44-(1276)-600-081
FDA Registration: 1000234991  Annual Revenues: USD 5-10 Million  Employee Count: ~30  Quality: ISO 9001, ISO13485 Certified
Products: Clostridium Difficile Antigen (FDA Code: MCB), Enzyme Immunoassay Test, Reticulocyte Stain (FDA Code: GJH), Whole Blood Plasma (FDA Code: DGQ), Radial Immunodiffusion Plates and Equipment (FDA Code: JZQ), Adenovirus 1-33 CF Antisera (FDA Code: GOA), ...
Microgen Bioproducts Ltd. develops, manufactures and sells products which are used by laboratory professionals to aid the detection & diagnosis of diseases & organisms which pose a threat to human and more...
 EMAIL INQUIRY to  5 Clostridium Difficile Antigen suppliers  
FDA Code / Regulation: MCB / 866.2660

A microorganism differentiation and identification device is a device 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.

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 866.9.

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