BEUDAMED
    3 results · 18ms · 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 ×

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 5, 2014

    XIA 3 TITANIUM TORQUE WRENCH SHORT

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code LXH·October 24, 2012

    CAROTID WALLSTENT MONORAIL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIM·September 1, 2010