
Abbott Ellipse DR Dual-Chamber ICD | REF CD2377-36C
Abbott Ellipse DR dual-chamber implantable cardioverter defibrillator (REF CD2377-36C) designed for atrial and ventricular sensing, pacing, and tachyarrhythmia therapy delivery.

The Medtronic Visia AF MRI ICD (REF DVFB1D1) is a single-chamber implantable cardioverter defibrillator engineered to deliver high-energy defibrillation therapy for patients at risk of life-threatening ventricular tachyarrhythmias. Built on Medtronic's SureScan platform, the Visia AF MRI integrates atrial fibrillation detection capabilities into a single-chamber device, supporting clinicians in monitoring AF burden without the need for an atrial lead.
Key Features
- Single-chamber ICD with integrated AF detection via the ventricular lead
- MRI SureScan technology for MR-conditional scanning under specified conditions
- High-voltage defibrillation therapy with programmable VT/VF detection zones
- SmartShock discrimination algorithms designed to help reduce inappropriate shocks
- OptiVol and CareAlert notifications (where supported by configuration)
- Compatible with Medtronic CareLink remote monitoring
- Anti-tachycardia pacing (ATP) and bradycardia pacing support
Clinical Applications
- Primary and secondary prevention of sudden cardiac death in indicated patients
- Management of ventricular tachycardia and ventricular fibrillation
- Monitoring of atrial fibrillation episodes and AF burden in single-chamber ICD recipients
- Patient populations requiring access to MR-conditional cardiac rhythm devices under labeled scanning conditions
Product Information
- Brand: Medtronic
- Model / Family: Visia AF MRI / Visia AF ICD
- REF / UPN: DVFB1D1
- Category: Implantable Cardioverter Defibrillators (ICD)
- Configuration: Single-chamber ICD
- MRI Status: MR-conditional under Medtronic SureScan labeled conditions
- Connector: Not specified in the located sources
- Dimensions / Weight / Longevity: Not specified in the located sources
- Sterility & Storage: Refer to manufacturer IFU
- Use: Prescription device; for use by qualified implanting physicians in accordance with the official Instructions for Use
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