BEUDAMED
    71 results · 37ms · Sources: EU EUDAMED, US FDA

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    VENTAK PRX

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·February 8, 1998

    SIMILAR DEVICE BNI75TCDDH, PMA # P030031

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·October 2, 2017

    SIMILAR DEVICE DI7TCBLRT, PMA # P030031

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·February 9, 2015

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

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

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

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

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

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

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

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

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 16, 1997

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 9, 1997

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 9, 1997

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 9, 1997

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 9, 1997

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 9, 1997

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 16, 1997

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026