
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 DR Dual-Chamber ICD (REF CD2359-36Q) is an implantable cardioverter defibrillator developed by Abbott (formerly St. Jude Medical) for patients indicated for dual-chamber defibrillation therapy. The device combines high-voltage tachyarrhythmia therapy with dual-chamber bradycardia pacing in a single pulse generator, intended to support clinicians in managing ventricular tachycardia and ventricular fibrillation while providing atrial sensing and pacing capabilities.
Key Features
- Dual-chamber configuration with atrial and ventricular sensing and pacing channels.
- High-voltage defibrillation therapy for ventricular tachyarrhythmia termination.
- DF-1/IS-1 lead connector platform for compatibility with compatible Abbott/St. Jude defibrillation and pacing leads.
- SenseAbility technology designed to support reliable sensing across a range of signal amplitudes.
- DeFT Response technology offering programmable shock waveform and polarity options.
- Diagnostic data logging including arrhythmia episode storage and intracardiac electrograms.
- Compatibility with Merlin@home and Merlin.net remote monitoring (verify with current Abbott documentation).
Clinical Applications
- Intended for use in patients meeting clinician-determined indications for dual-chamber ICD therapy.
- Detection and treatment of ventricular tachycardia (VT) and ventricular fibrillation (VF).
- Bradycardia pacing support in the atrium and ventricle.
- Long-term arrhythmia monitoring and follow-up via compatible programmer and remote care systems.
Product Information
- Brand: Abbott (St. Jude Medical legacy platform)
- Model Family: Fortify Assura DR
- REF/UPN: CD2359-36Q
- Category: Implantable Cardioverter Defibrillators (ICD)
- Configuration: Dual-chamber (atrial + ventricular)
- Connector Standard: DF-1 / IS-1
- Device Dimensions / Mass / Volume: Not specified in the located sources
- Battery Longevity: Not specified in the located sources
- MRI Conditional Status: Not specified in the located sources
- Sterility: Supplied sterile for single use; verify packaging and expiration prior to implantation.
- Regulatory Status: Not specified in the located sources; confirm regional clearance with Abbott prior to procurement.
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