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

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    Medtronic, Temporary Pacing Lead System, Model 6416, Sterile EO. Product Catalog Numbers: Five (5) Pack Single Pack 6416-100 6416-1005 6416-140 6416-1405 6416-200 6416-2005 For temporary intracardiac pacing and EGM recording. The system is disposable, for temporary single patient use, with a contemplated implant duration of 7 days or less. The system is used with Medtronic temporary external pacemakers.

    FDA Recall
    Terminated ·Medtronic Inc., Cardiac Rhythm and Heart Failure·Product code LDF·June 16, 2016

    Patient Cart, Part: 380601, a component of the da Vinci SP Surgical System, Model: SP1098

    FDA Recall
    Open, Classified ·Intuitive Surgical, Inc.·Product code NAY·March 13, 2024

    PROPONENT SR Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017

    VALITUDE CRT-P Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code NKE·December 7, 2017

    ACCOLADE MRI DR Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017

    ESSENTIO EL DR Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017

    VISIONIST X4 CRT-P Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code NKE·December 7, 2017

    VISIONIST CRT-P Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code NKE·December 7, 2017

    ESSENTIO SR Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017

    VALITUDE X4 CRT-P Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code NKE·December 7, 2017

    PROPONENT DR Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017

    ACCOLADE EL DR Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017

    ACCOLADE SR Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017

    ESSENTIO MRI SR Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017

    ACCOLADE MRI SR Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017

    ALTRUA 2 SR Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017

    PROPONENT EL DR Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017

    PROPONENT MRI Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017

    ESSENTIO MRI EL DR Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017

    ACCOLADE DR Pacemaker

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code LWP·December 7, 2017