BEUDAMED
    3 results · 26ms · 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 FDA Adverse Event ×

    REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 10

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 11, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·December 1, 2010

    5.0MM CANNULATED LOCKING SCREW80MM

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·July 3, 2014