BEUDAMED
    6 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ENDOTAK PLUS TRANSVENOUS DEFIBRILLATION LEAD IS-1

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS·Product code LWS·September 8, 1997

    VENTAK PRX III IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS·Product code LWS·September 8, 1997

    VENTAK MINI II HC

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·September 8, 1997

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 9, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 1, 2007

    TECNIS

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code MFK·October 24, 2012