BEUDAMED
    3 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 FDA Adverse Event ×

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS , INNOVATION CENTER - SILICON VALLEY·Product code GEX·October 28, 2010

    CURRENT PLUS VR, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC. CRMD·Product code LWS·January 13, 2014

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 31, 2012