BEUDAMED
    7 results · 17ms · 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.

    AEQUITRON MED-7100 PHOTOTHERAPY LIGHT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209100149·KIT, EAGLE IFAK - CELOX GAUZE - BLK

    MEDIGLOVES STERILE POWDER-FREE SYNTHETIC POLYISOPRENE SURGICAL GLOVES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    AV Viewer

    FDA 510(k)
    FDA Class 2 ·Radiology

    BONE SCREW, T7, DIAM. 2.7X16MM

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code HRS·June 5, 2014

    SPEEDLOCK KNOTLESS IMPLANT

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code MBI·November 21, 2012

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FPO·September 22, 2010