
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 Ellipse VR Single-Chamber ICD (REF CD1377-36QC) is an implantable cardioverter defibrillator engineered for the detection and treatment of ventricular tachyarrhythmias. As part of Abbott's Ellipse VR platform, the device combines a compact, contoured titanium housing with established sensing and high-voltage therapy capabilities intended to support long-term device-based management of patients at risk of sudden cardiac death.
Key Features
- Single-chamber ICD configuration for right ventricular sensing, pacing, and defibrillation therapy
- Contoured, low-profile titanium can designed to support pectoral implantation
- Programmable bradycardia pacing, anti-tachycardia pacing (ATP), cardioversion, and defibrillation therapies
- DF-1 / IS-1 lead connector configuration (verify against current Abbott technical manual)
- Compatible with Abbott Merlin@home remote monitoring and Merlin Patient Care System (PCS) programmer
- Diagnostic data storage including stored electrograms and arrhythmia episode logs
- MRI conditional labeling status: Not specified in the located sources — refer to current Abbott MRI Ready documentation
Clinical Applications
- Primary and secondary prevention of sudden cardiac death in adult patients meeting accepted indications for single-chamber ICD therapy
- Detection and termination of ventricular tachycardia (VT) and ventricular fibrillation (VF) via ATP and high-voltage shock therapy
- Backup bradycardia pacing in the right ventricle
- Long-term ambulatory rhythm surveillance via remote monitoring workflows
Product Information
- Brand: Abbott (formerly St. Jude Medical)
- Product Family: Ellipse VR Single-Chamber ICD
- REF / UPN: CD1377-36QC
- Category: ICD Devices | Implantable Cardioverter Defibrillators
- Device Type: Single-chamber implantable cardioverter defibrillator (VR)
- Connector Standard: DF-1 / IS-1 (confirm with Abbott technical specifications)
- Battery Chemistry / Longevity: Not specified in the located sources
- Device Dimensions / Mass / Volume: Not specified in the located sources
- Sterility: Supplied sterile for single use; do not resterilize
- Storage: Store per manufacturer's Instructions for Use
- Regulatory Status: Not specified in the located sources — verify country-specific clearance prior to procurement
- Always consult the current Abbott Instructions for Use (IFU) and clinician's manual for complete specifications, indications, contraindications, warnings, and precautions.
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