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 ×

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·January 15, 2013

    PERMANENT CAUTERY SPATULA INSTRUMENT

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL,INC.·Product code NAY·July 23, 2014

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·January 21, 2011