BEUDAMED
    7 results · 22ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    INFINITI™ Ambi Angiographic Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Symmetry Cobb

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482001677·Symmetry® Curette, Cobb, Size 1, Tip 3.5 mm Wid...

    DIMENSION PROCAINAMIDE (PROC) FLEX REAGENT CARTRIDGE METHOD, MODEL DF110

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    VITEK 2 AST ST MOXIFLOXACIN, VITEK 2 AST STREPTOCOCCUS MOXIFLOXACIN

    FDA 510(k)
    FDA Class 2 ·Microbiology

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·November 13, 2008

    COMPOSIX MESH E/X

    FDA Adverse Event
    Injury ·DAVOL INC·Product code FTL·August 24, 2011

    GYNECARE PROSIMA PELVIC FLOOR REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·July 18, 2013