
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 Abbott Fortify Assura VR Single-Chamber Implantable Cardioverter Defibrillator (ICD), REF CD1359-40Q, is a single-chamber defibrillation device engineered to detect ventricular tachyarrhythmias and deliver appropriate antitachycardia pacing, cardioversion, or defibrillation therapy. Originally developed under St. Jude Medical and now part of the Abbott cardiac rhythm management portfolio, the Fortify Assura platform supports physicians managing patients at risk of sudden cardiac arrest with a focus on device longevity, programmable detection algorithms, and streamlined follow-up.
Key Features
- Single-chamber VR ICD configuration with one right ventricular lead port
- High-energy defibrillation output for ventricular tachycardia and ventricular fibrillation therapy
- Programmable antitachycardia pacing (ATP) and bradycardia pacing support
- DF4 connector compatibility for streamlined lead connection (verify on device label)
- SecureSense Lead Noise Discrimination algorithm to help reduce inappropriate shocks
- TailoredTherapy programmable detection and therapy parameters
- Compatible with the Merlin Patient Care System and Merlin@home remote monitoring
- Compact titanium housing designed for pectoral implantation
Clinical Applications
- Primary and secondary prevention of sudden cardiac death in indicated patients
- Detection and termination of ventricular tachycardia (VT)
- Detection and termination of ventricular fibrillation (VF)
- Backup bradycardia pacing in patients without an indication for atrial pacing
- Long-term cardiac rhythm management with remote follow-up workflows
Product Information
- Brand: Abbott (formerly St. Jude Medical)
- Product Family: Fortify Assura
- Model / REF: CD1359-40Q
- Device Type: Single-Chamber Implantable Cardioverter Defibrillator (VR ICD)
- Category: ICD Devices | Implantable Cardioverter Defibrillators
- Connector: DF4/IS-1 configuration (Not specified in the located sources for this exact suffix; verify on device label)
- Maximum Delivered Energy: Not specified in the located sources
- Sterility: Supplied sterile for single use
- Storage: Per manufacturer Instructions for Use (IFU)
- Regulatory Status: Refer to Abbott labeling and local regulatory authorities for market-specific clearance
- Intended Users: Qualified implanting physicians and cardiac electrophysiology centers
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