BEUDAMED
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    Tachos DR - Implantable Cardioverter Defibrillator.

    FDA Recall
    Terminated ·Biotronik Inc·Product code LWS·February 21, 2003

    Lumax Cardiac Resyncronization Therapy Defibrillator (CRT-D); Implantable, dual-chamber defibrillator; Model Number: HF-T; Catalog Number 355263; Software Version 603.U; Catalog Model Number 359251; ICS 3000 units are composed of three Catalog/Model Numbers: 349527, 349530, and 355547. The model 349530 is the component which is loaded/updated with software.

    FDA Recall
    Terminated ·Biotronik Inc·Product code MRM·January 10, 2007

    BIOTRONIK Ilestro 7 VR-T, DF-1, REF 383578, UDI: 04035479125349 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.

    FDA Recall
    Terminated ·BIOTRONIK Inc·Product code MRM·March 8, 2021

    BIOTRONIK ITREVIA 7, VR-T DF-4, REF 393041, UDI: 04035479129569 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.

    FDA Recall
    Terminated ·BIOTRONIK Inc·Product code MRM·March 8, 2021

    BIOTRONIK ILIVIA 7, VR-T DF-1 ProMRI, REF 404625, UDI: 04035479142124 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.

    FDA Recall
    Terminated ·BIOTRONIK Inc·Product code MRM·March 8, 2021

    BIOTRONIK ILIVIA 7, DR-T DF4 ProMRI, REF 404623, UDI: 04035479142100 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.

    FDA Recall
    Terminated ·BIOTRONIK Inc·Product code MRM·March 8, 2021

    PSW 1203.U/1, PSW 1301.U, PSW 1307.U, PSW 1403.U, and PSW 1501.U Pacemaker Programmer software. Software approved for use with BIOTRONIK device programmers (trade names: Renamic and ICS 3000). Allows physicians to program devices to pace exclusively in the left ventricle.

    FDA Recall
    Terminated ·BIOTRONIK, Inc.·Product code rce·June 30, 2015

    Belos VR Implantable Cardioverter Defibrillator

    FDA Recall
    Terminated ·Biotronik Inc·Product code LWS·September 24, 2003

    BIOTRONIK INTICA NEO 7 HF-T DF-1 IS-1 ProMRI, REF 429553, UDI: 04035479156831 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.

    FDA Recall
    Terminated ·BIOTRONIK Inc·Product code LWS·March 8, 2021

    BIOTRONIK ILIVIA 7, VR-T DF4 ProMRI, REF 404626, UDI: 04035479142131 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.

    FDA Recall
    Terminated ·BIOTRONIK Inc·Product code MRM·March 8, 2021

    Deikos A+

    FDA Recall
    Terminated ·Biotronik Inc·Product code LWS·April 29, 2004

    BIOTRONIK ILIVIA NEO 7 DR-T DF-1 ProMRI, REF 429529, UDI: 04035479156749 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.

    FDA Recall
    Terminated ·BIOTRONIK Inc·Product code LWS·March 8, 2021

    BIOTRONIK Iforia 7,DR-T, DF-1,REF 390064, UDI: 04035479126926 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.

    FDA Recall
    Terminated ·BIOTRONIK Inc·Product code MRM·March 8, 2021

    BIOTRONIK INTICA NEO 7 VR-T DX DF-1 ProMRI, REF 429559, UDI: 04035479156855 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.

    FDA Recall
    Terminated ·BIOTRONIK Inc·Product code LWS·March 8, 2021

    Belos VR-T implantable cardioverter defibrillator. Implantable Cardioverter Defibrillator. The Belos VR-T is a single-chamber implantable cardioverter defibrillator (ICD) that detects and treats ventricular tachyarrhythmias and provides rate adaptive bradycardia pacing support. The ICDs are designed to collect diagnostic data to aid the physician''s assessment of a patient''s condition and the performance of the implanted device.

    FDA Recall
    Terminated ·Biotronik Inc·Product code LWS·March 21, 2003

    Belos DR Implantable Cardioverter Defibrillator

    FDA Recall
    Terminated ·Biotronik Inc·Product code LWS·September 24, 2003

    Belos VR-T Implantable Cardioverter Defibrillator

    FDA Recall
    Terminated ·Biotronik Inc·Product code LWS·September 24, 2003

    Tachos DR - Atrial TX Implantable Cardioverter Defibrillators

    FDA Recall
    Terminated ·Biotronik Inc·Product code LWS·February 21, 2003

    Belos DR-T Implantable Cardioverter Defibrillator

    FDA Recall
    Terminated ·Biotronik Inc·Product code LWS·September 24, 2003

    BIOTRONIK Ilestro 7 DR-T, DF-4, REF383564, UDI: 04035479125202 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.

    FDA Recall
    Terminated ·BIOTRONIK Inc·Product code MRM·March 8, 2021