BEUDAMED
    5 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ENDOTAK C TRANSVENOUS DEFIBRILLATION LEAD

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

    VENTAK PRX III IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

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

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·December 5, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 19, 2011

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    UNKNOWN·Product code ITJ·July 29, 2013