BEUDAMED
    3 results · 29ms · 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 ×

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·April 11, 2013

    LINOX S 65

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code LWS·March 15, 2011

    REFLOTRON PLUS V

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GKZ·May 22, 2008