One Becton Drive, Franklin Lakes, New Jersey 07417, USA www.bd.com/us
FDA Registration: 1119779 Annual Revenues:
USD 10-25 Million Employee Count:
ISO 9000, CE Certified
: Software Programs, CCD Cameras, & Gamma Cameras, Biomedical Devices, 3D Imaging Devices, Frame Grabbers, Densitometers Accessories, ...
Becton, Dickinson & Co., manufactures and distributes a broad range of medical supplies, devices, laboratory equipment and diagnostic products. Our product BD Soluvia™ is a prefillable microinje more...
2280 Sutherland Avenue, Suite 101, Knoxville, Tennessee 37919-2326, USA www.gryphus.com
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+1-(865)-251-0101, 800- 924-419
FDA Registration: 3006546675 Year Established:
: Periodontal Probes, Influenza Virus Antisera (FDA Code: GNS
), Candida Albicans ID Antigen (FDA Code: LHK
), Trichomonas Vaginalis Dna Probe (FDA Code: MJK
), Bacterial Sialidase Vaginal Test (FDA Code: MXB
), Diagnostic Rapid Test Kits, ...
Gryphus Diagnostics, LLC specializes in development and manufacture of rapid detection systems. Our products is BVblue® rapid tests for bacterial vaginosis. Our BVblue® is for use in the clini more...
Khan Street Amanat Pura, Jammu Road, Sialkot, Punjab 51310, Pakistanwww.landentools.com
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: Laser Power Probe, Laparoscopic Probes, Periodontal Probes, Medical Probes (FDA Code: HXB
), Guiding Probes, Probes (FDA Code: HXB
Landen Tools Inc. specializes in producing custom medical and beauty tools. Our medical products include anesthesia instruments, diagnostic instruments, forceps and general instruments. We offer medic more...
FDA Code / Regulation: MJK / 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.