BEUDAMED
    3 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 FDA Adverse Event ×

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 14, 2012

    EXACTAMIX NON-VENTED HIGH-VOLUME INLET

    FDA Adverse Event
    BAXTER HEALTHCARE CORP·Product code LHI·September 3, 2013

    ATTAIN STARFIX

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·June 10, 2015