
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 Epsila EV MRI SureScan Extravascular ICD Lead (REF EV2401) is an implantable defibrillation lead engineered for substernal placement as part of the Aurora EV-ICD extravascular defibrillator system. By routing the lead beneath the sternum rather than through the vasculature, this design aims to deliver high-energy defibrillation therapy and pacing functionality while preserving venous access and avoiding the leads being placed inside the heart or veins.
Key Features
Extravascular lead architecture intended for substernal positioning outside the heart and vasculature.
Supports defibrillation therapy plus anti-tachycardia pacing (ATP) and pause-prevention pacing when used with a compatible Aurora EV-ICD pulse generator.
MRI SureScan labeling intended to support conditional use in the magnetic resonance environment when full system conditions are met.
Multi-electrode configuration including defibrillation coil(s) and pace/sense electrodes along the distal segment.
Designed for implantation via a dedicated Medtronic substernal tunneling tool set.
DF4 high-voltage connector configuration for compatibility with the Aurora EV-ICD generator.
Clinical Applications
Component of an extravascular implantable cardioverter defibrillator system for patients indicated for ICD therapy.
Intended to provide defibrillation of ventricular tachyarrhythmias.
Intended to provide anti-tachycardia and post-shock pacing capability without an endocardial lead.
Suited to clinical strategies that aim to preserve the venous system and avoid intracardiac or subcutaneous-only lead placement.
Product Information
Brand: Medtronic
Model / Family: Epsila EV MRI SureScan
REF / UPN: EV2401
Category: ICD Devices | Implantable Cardioverter Defibrillators (Extravascular ICD Lead)
Lead type: Extravascular (substernal) defibrillation and pace/sense lead
Connector: DF4 (compatible with Aurora EV-ICD generator)
MRI status: MRI SureScan conditional when implanted as part of a complete labeled system; refer to current IFU for conditions
Lead length / electrode spacing / fixation details: Not specified in the located sources
Sterility & single use: Supplied sterile for single use; do not resterilize unless stated in the official IFU
Regulatory status & market availability: Refer to Medtronic for region-specific approval and availability
Documentation: Always consult the current Medtronic Instructions for Use and product manual prior to clinical use
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.