BEUDAMED
    3 results · 19ms · 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 ×

    HEARTSTART XL+ DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 21, 2014

    AUTOCAT2 WAVE

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DSP·October 8, 2010

    HAKIM PROGRAMMABLE VALVE

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF - MEDOS·Product code JXG·December 20, 2012