BEUDAMED
    3 results · 17ms · 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 ×

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 21, 2014

    UNKNOWN DEPUY FEMORAL HEAD

    FDA Adverse Event
    Malfunction ·DEPUY INTERNATIONAL·Product code KXA·September 26, 2012

    MARATHON MICRO CATHETER

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code KRA·July 8, 2010