BEUDAMED
    6 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OPTIQ CATHETER

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FPA·September 4, 2014

    OPTIQ CATHETER

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FPA·September 4, 2014

    SCORPIO-FLEX PS X3 TIB INSERT

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·April 14, 2014

    HEARTSTART MRX -EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 2, 2008

    SABINA

    FDA Adverse Event
    Malfunction ·LIKO AB·Product code FSA·September 9, 2011

    FLOGARD

    FDA Adverse Event
    Malfunction ·SHARP CORPORATION OSAKA JAPAN·Product code FRN·July 29, 2013