
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 Cobalt ICD (REF DDPB3D4) is a dual-chamber implantable cardioverter defibrillator from Medtronic's Cobalt platform, engineered to deliver antitachycardia pacing, cardioversion and defibrillation therapy for patients at risk of ventricular tachyarrhythmias and sudden cardiac arrest. The device integrates bradycardia pacing support with advanced arrhythmia discrimination to help reduce inappropriate shocks in routine clinical practice.
Key Features
- Dual-chamber ICD configuration with atrial and ventricular sensing, pacing and high-voltage therapy capabilities.
- SmartShock discrimination algorithms intended to differentiate supraventricular from ventricular tachyarrhythmias.
- Supports BlueSync wireless technology for communication with compatible programmers and remote monitoring platforms.
- Designed for 1.5T and 3T MRI conditional scanning when implanted as part of a compatible SureScan system (confirm with current labeling).
- Onboard diagnostics including arrhythmia episode storage, EGM recordings and device performance trends.
- Compatible with the Medtronic CareLink network for remote follow-up workflows.
Clinical Applications
- Primary and secondary prevention of sudden cardiac death in indicated patient populations.
- Management of documented ventricular tachycardia and ventricular fibrillation.
- Dual-chamber bradycardia pacing support in patients requiring atrial and ventricular pacing.
- Long-term rhythm monitoring and remote device surveillance in electrophysiology and cardiology programs.
Product Information
- Brand: Medtronic
- Model / Family: Cobalt DR ICD
- REF / UPN: DDPB3D4
- Category: Implantable Cardioverter Defibrillators (ICD)
- Configuration: Dual-chamber (DR)
- Connector: Not specified in the located sources
- Dimensions / Weight / Volume: Not specified in the located sources
- Battery longevity: Not specified in the located sources
- Sterility / Single use: Supplied sterile, single-use implantable device
- Regulatory status: Refer to current manufacturer labeling and local regulatory clearances prior to use.
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