BEUDAMED
    11 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    FORTIFY ASSURA VR ICD_IDE_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·September 29, 2025

    ELLIPSE VR ICD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017

    CD2257-40Q FORTIFY ASSURA DR ICD_IDE_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NVZ·June 14, 2017

    FORTIFY ASSURA VR ICD_IDE_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code NVZ·October 31, 2017

    FRESENIUS 2008K

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 25, 2014

    LAMITRODE 44

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 22, 2013

    FORTIFY ST DR, U1.6 SJ4 ID

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code LWS·January 18, 2017

    FORTIFYASSURA DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·January 3, 2017

    FORTIFY ASSURA VR ICD_O_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·January 27, 2016

    CONTOUR II V-185 AC SERIES TIERED THERAPY DEFIB

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code LWS·November 26, 1999