BEUDAMED
    4 results · 15ms · 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 Status: Malfunction ×

    INSET GUARD

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·March 30, 2026

    ATLANTIS SR PRO2 CORONARY IMAGING CATHETER, MODEL 39014

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT·Product code DQO·February 28, 2011

    2250051-2008-00093

    FDA Adverse Event
    Malfunction ·Product code JTC·February 11, 2008

    CARDIOSAVE HYBRID, TYPE I PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·July 18, 2025