BEUDAMED
    224 results · 176ms · Sources: EU EUDAMED, US FDA

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    CABLE, PACEMAKER, EXTERNAL, SINGLE USE

    FDA Adverse Event
    Other ·MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT·Product code LDF·May 9, 2012

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT·Product code LWS·May 9, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT·Product code DTB·May 9, 2013

    CAPSURE SENSE LEAD,

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT·Product code NVN·August 12, 2023

    SELECTSECURE MRI SURESCAN LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT·Product code NVN·May 8, 2024

    CAPSURE SP NOVUS LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT·Product code NVN·May 8, 2024

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT·Product code LWS·November 15, 2012

    CAPSURE SP NOVUS LEAD

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT·Product code NVN·October 2, 2024

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT·Product code LWS·August 23, 2013

    Medtronic Sprint Fidelis 6949 Steroid eluting, quadripolar, screw-in, ventricular lead with right ventricular (RV) / Superior Vena Cava (SVC) defibrillation coil electrodes. Sterile. This lead is designed for pacing, sensing, cardioversion and defibrillation therapies. Medtronic World Headquarters, Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA.

    FDA Recall
    Terminated ·Medtronic Inc. Cardiac Rhythm Managment·Product code LWS·October 15, 2007

    Medtronic Sprint Fidelis 6948 Steroid eluting, quadripolar, ventricular lead with tined tip and right ventricular (RV) / Superior Vena Cava (SVC) defibrillation coil electrodes. Sterile. This lead is designed for pacing, sensing, cardioversion and defibrillation therapies. Medtronic World Headquarters, Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA.

    FDA Recall
    Terminated ·Medtronic Inc. Cardiac Rhythm Managment·Product code LWS·October 15, 2007

    Medtronic Sprint Fidelis 6931 Steroid eluting, tripolar, screw-in, ventricular lead with right ventricular (RV) defibrillation coil electrode. Sterile. This lead is designed for pacing, sensing, cardioversion and defibrillation therapies. Medtronic World Headquarters, Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA.

    FDA Recall
    Terminated ·Medtronic Inc. Cardiac Rhythm Managment·Product code LWS·October 15, 2007

    Medtronic Sprint Fidelis 6930 Steroid eluting, tripolar, ventricular lead with tined tip and right ventricular (RV) defibrillation coil electrode. Sterile. This lead is designed for pacing, sensing, cardioversion and defibrillation therapies. Medtronic World Headquarters, Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA.

    FDA Recall
    Terminated ·Medtronic Inc. Cardiac Rhythm Managment·Product code LWS·October 15, 2007

    MEDTRONIC CAPSURE(R) SP MODEL 5524M PACING LEADS

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIAC RHYTHM DISEASE, MANAGEMENT / MEDTRONIC INC.·Product code DTB·June 16, 2025

    CROME VR ICD MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT/MEDTRONIC INC.·Product code LWS·January 9, 2025

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC INC., CARDIAC RHYTHM DISEASE MANAGEMENT·Product code LWS·February 23, 2010

    SPRINT FIDELIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC INC., CARDIAC RHYTHM DISEASE MANAGEMENT·Product code LWS·March 5, 2010

    ATTAIN OTW

    FDA Adverse Event
    Malfunction ·MEDTRONIC INC., CARDIAC RHYTHM DISEASE MANAGEMENT·Product code OJX·January 17, 2010

    SPRINT FIDELIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC INC., CARDIAC RHYTHM DISEASE MANAGEMENT·Product code LWS·February 8, 2010

    SPRINT FIDELIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC INC., CARDIAC RHYTHM DISEASE MANAGEMENT·Product code LWS·January 22, 2010