BEUDAMED
    3 results · 34ms · 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·March 25, 2014

    UNKNOWN LEFT HIP

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·October 30, 2012

    ENVOY 6F GUIDING CATHETERS

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DQY·September 14, 2010