
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 DDPB3D1) is an implantable cardioverter defibrillator from the Cobalt platform, engineered to provide automated detection and treatment of ventricular tachyarrhythmias. It integrates Medtronic's BlueSync technology to support wireless communication with compatible programmers and remote monitoring systems, helping streamline device follow-up workflows in cardiac electrophysiology programs.
Key Features
Dual-chamber ICD platform within the Medtronic Cobalt family.
BlueSync wireless connectivity for in-clinic and remote device interrogation.
SmartShock detection algorithms intended to help discriminate between ventricular and supraventricular arrhythmias.
TherapyGuide and programming assistance features to support device parameter selection.
MRI access conditions documented in the device technical manual.
Compatible with the Medtronic CareLink remote monitoring network.
Clinical Applications
Management of patients indicated for an implantable cardioverter defibrillator under physician assessment.
Detection and termination of ventricular tachycardia and ventricular fibrillation episodes.
Bradycardia pacing support as configured by the implanting physician.
Long-term device follow-up via wireless remote monitoring workflows.
Product Information
Brand: Medtronic
Model Family: Cobalt ICD
REF / UPN: DDPB3D1
Category: ICD Devices | Implantable Cardioverter Defibrillators
Device Type: Implantable cardioverter defibrillator (Cobalt platform)
Connectivity: BlueSync wireless telemetry; CareLink remote monitoring compatible
Header / Lead Configuration: Not specified in the located sources
Battery Longevity: Not specified in the located sources
Device Dimensions and Mass: Not specified in the located sources
MRI Conditions: Refer to the official Medtronic device manual for current MR conditional labeling and scanning conditions
Sterility: Supplied sterile for single use; do not resterilize
Intended Users: Trained cardiac electrophysiologists and implanting physicians
Documentation: Use only in accordance with the official Medtronic Instructions for Use and technical manual
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.