BEUDAMED
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    Filters FDA Adverse Event ×

    SMITH & NEPHEW

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code GEI·November 12, 2014

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·August 10, 2011

    OT PING METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 30, 2013