BEUDAMED
    6 results · 19ms · 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 ×

    UNILYTE A

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SpineAR SNAP (SyncAR Spine)

    FDA 510(k)
    FDA Class 2 ·Neurology

    Narval Brux

    FDA 510(k)
    FDA Unclassified ·Unknown

    VENACURE NEVERTOUCH DIRECT

    FDA Adverse Event
    Injury ·ANGIODYNAMICS·Product code GEX·May 27, 2014

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·October 25, 2012

    BIPHASIC LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·September 22, 2010