BEUDAMED
    4 results · 22ms · 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 ×

    4905510

    FDA Adverse Event
    Death ·July 10, 2015

    CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 28, 2014

    FLEXTEND

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVN·January 9, 2013

    HYLAMER 10D 56 OR 68ODX28ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDL·November 19, 2010