Dermatophyte Identification Kit Suppliers
EMAIL INQUIRY to 1 suppliers
Bio-Med Diagnostics, Inc. | Address: 1388 Antelope Road, White City, Oregon 97503-1619, USA 
www.biomed1.com | Send Inquiry | Phone: +1-(541)-830-3000
FDA Registration: 2951280 Year Established: 1989 Annual Revenues: < USD 1 Million Quality: ISO 13485:2003, CE Certified
Products: Laboratory Equipment, Gonorrhea Test Kits, Swabs, Gonorrhea Test Kits, Laboratory Equipment, Incubator Chambers, Laboratory Equipment, Kimura Spatulas, Laboratory Equipment Thermal Shakers, ...
Bio-Med Diagnostics, Inc. develops and markets gold standard in-vitro diagnostic products for the detection of infectious diseases & fungi in the human clinical & industrial markets. We manufacture di more...
www.biomed1.com | Send Inquiry | Phone: +1-(541)-830-3000
FDA Registration: 2951280 Year Established: 1989 Annual Revenues: < USD 1 Million Quality: ISO 13485:2003, CE Certified
Products: Laboratory Equipment, Gonorrhea Test Kits, Swabs, Gonorrhea Test Kits, Laboratory Equipment, Incubator Chambers, Laboratory Equipment, Kimura Spatulas, Laboratory Equipment Thermal Shakers, ...
Bio-Med Diagnostics, Inc. develops and markets gold standard in-vitro diagnostic products for the detection of infectious diseases & fungi in the human clinical & industrial markets. We manufacture di more...
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EMAIL INQUIRY to 1 Dermatophyte Identification Kit suppliers
FDA Code / Regulation: JSR / 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.
