BEUDAMED
    3 results · 33ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 6, 2010

    ZIPWIRE HYDROPHILIC GUIDE WIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQX·January 17, 2013

    ENDURITY DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·July 8, 2014