
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 DVPB3D4) is an implantable cardioverter defibrillator from Medtronic's Cobalt platform, designed to deliver tachyarrhythmia detection and therapy together with bradycardia pacing support. This catalog listing is intended for qualified B2B procurement, hospital supply chain, and authorized distributor channels.
Key Features
Dual-chamber ICD configuration supporting atrial and ventricular sensing and pacing.
High-voltage defibrillation therapy with programmable shock energy.
Antitachycardia pacing (ATP) capabilities for ventricular tachyarrhythmias.
BlueSync technology supporting wireless communication with compatible Medtronic programmers and remote monitoring ecosystems (per manufacturer documentation).
MRI-conditional labeling — refer to current Medtronic MRI Technical Manual for scan conditions.
Designed for use with compatible Medtronic transvenous defibrillation and pacing leads.
Longevity and battery performance details: Not specified in the located sources.
Clinical Applications
Intended for patients meeting accepted indications for implantable cardioverter defibrillator therapy, including primary and secondary prevention of sudden cardiac death.
Supports management of ventricular tachycardia and ventricular fibrillation through detection, ATP, cardioversion, and defibrillation.
Provides bradycardia pacing support where clinically indicated.
Final clinical suitability is determined solely by the implanting physician in accordance with the official Medtronic Instructions for Use (IFU) and applicable local regulatory labeling.
Product Information
Brand: Medtronic
Product Family: Cobalt ICD
Model / REF: DVPB3D4
Category: Implantable Cardioverter Defibrillators (ICD)
Configuration: Dual-chamber ICD
Connector Type: Not specified in the located sources
Dimensions / Weight / Volume: Not specified in the located sources
Sterility: Supplied sterile for single use, per manufacturer labeling
Storage: Refer to manufacturer IFU
Regulatory: Refer to current Medtronic labeling and local regulatory authority for market-specific approval status
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