BEUDAMED
    562 results · 26ms · Sources: EU EUDAMED, US FDA

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    FORTIFY ASSURA DR ICD, US

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·June 13, 2016

    FORTIFY ASSURA VR ICD_IDE_US

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

    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

    UNIFY ASSURA CRT-D RF HV

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWS·March 29, 2019

    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

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·CADENCE(R) TIERED THERAPY DEFIBRILLATION SYSTEM

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·CADENCE FAMILY OF ICDS

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·CADENCE/CADET/CONTOUR/CONTOUR II/MD/ATLAS II/MD/PROFILE II/MD/PHOTON/PHOTON MICRO/CURRENT/+/ATLAS II/+/EPIC II/+/CONVERT

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·CADENCE(R) TIERED THERAPY DEFIBRILLATOR SYSTEM

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTRITEX HOUSECALL RECEIVER/TRANSMITTER

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·FORTIFY AND FORTIFY ASSURA FAMILIES OF ICD DEVICES

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·CADET TIERED THERAPY DEFIBRILLATOR SYSTEM

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·FORTIFY ASSURA VR, FORTIFY ASSURA DR

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·CD1231-40, CD1231-40Q, CD2231-40, CD2231-40Q, CD1257-40, CD1257-40Q, CD2257-40, CD2257-40Q, CD1357-40, CD1357-40C, CD135

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Neutrino NxT VR, Gallant VR, Entrant VR, Neutrino NxT DR, Gallant DR, Entrant DR, Avant VR, Avant DR