
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 CD1377-36C) is an implantable cardioverter defibrillator engineered to detect and treat life-threatening ventricular tachyarrhythmias. Featuring a contoured, compact titanium housing and Abbott's proven sensing and therapy algorithms, the Ellipse VR is intended to support reliable long-term rhythm management while streamlining the implant procedure.
Key Features
- Single-chamber ICD platform for ventricular sensing, pacing and defibrillation therapy
- Compact, contoured can designed to facilitate pectoral implantation and patient comfort
- High-energy defibrillation with biphasic shock waveform
- SecureSense lead noise discrimination to help reduce inappropriate therapy
- DeFT Response programmable shock polarity and waveform tuning
- MRI-conditional labeling when implanted as part of a compatible system (verify per current IFU)
- Merlin@home and Merlin.net remote monitoring compatibility for longitudinal patient follow-up
- DF-1/IS-1 connector configuration for broad lead compatibility
Clinical Applications
- Management of patients at risk of sudden cardiac arrest due to ventricular tachycardia or ventricular fibrillation
- Primary and secondary prevention indications per physician assessment
- Delivery of antitachycardia pacing (ATP), cardioversion and defibrillation therapy
- Bradycardia backup pacing in the ventricle (VVI/VVIR)
- Long-term remote rhythm surveillance in chronic heart failure and post-MI populations
Product Information
- Brand: Abbott (formerly St. Jude Medical)
- Model / Family: Ellipse VR Single-Chamber ICD
- REF / UPN: CD1377-36C
- Category: ICD Devices | Implantable Cardioverter Defibrillators
- Device type: Single-chamber implantable cardioverter defibrillator
- Connector: DF-1 / IS-1 (verify per current IFU)
- Maximum delivered energy: Not specified in the located sources
- Dimensions / mass / volume: Not specified in the located sources
- Projected longevity: Not specified in the located sources
- MRI status: MRI-conditional when implanted as part of a compatible system; refer to current Abbott MRI-Ready labeling
- Sterility: Supplied sterile for single use
- Storage & handling: Store per manufacturer IFU
- Regulatory / clinical use: Refer to current Abbott Instructions for Use and local regulatory labeling
Tell us what product you need and share a few details.
We connect your request with the most relevant verified brands.
Relevant supplier options can respond with availability, documentation context, and quote details.
Practical answers for procurement teams reviewing this product page.
Include the exact product family, brand preference, REF/UPN code when available, required quantity, destination country, expected delivery timing and documentation expectations.
Yes. If alternatives are acceptable, mention equivalent brands, compatible models, size ranges and any non-negotiable requirements.
Related products are connected through structured catalog data such as brand, category, product family and country assignment.
No. This page supports sourcing and RFQ organization. Buyers must verify regulatory status, clinical suitability and procurement compliance independently.
Specific codes reduce ambiguity and help supplier teams identify product availability, packaging details and documentation faster.
Yes. The workflow is designed for hospitals, clinics, distributors, wholesalers, importers and procurement departments.
Yes. Products can be connected to multiple countries in the admin panel, and buyers can specify destination details in the RFQ form.
The request is stored with contact and procurement details so the sourcing conversation can be reviewed and followed up clearly.