Medtronic Aurora EV-ICD MRI SureScan Extravascular ICD | REF DVEA3E4

The Medtronic Aurora EV-ICD MRI SureScan (REF DVEA3E4) is an extravascular implantable cardioverter defibrillator engineered to provide defibrillation therapy with a lead positioned outside the heart and veins. The system is designed to treat ventricular tachyarrhythmias while avoiding transvenous lead placement, and is labeled as MRI SureScan to support magnetic resonance imaging under specified conditions.

Key Features
Extravascular ICD platform intended for use with a substernal defibrillation lead.
MRI SureScan labeling supporting MRI scanning under manufacturer-defined conditions of use.
Delivers defibrillation shocks for ventricular tachyarrhythmia therapy.
Supports anti-tachycardia pacing (ATP) and pause-prevention pacing as described in Medtronic labeling.
Designed for compatibility with the Medtronic CareLink remote monitoring ecosystem.
Engineered for streamlined implantation without intracardiac or transvenous leads.

Clinical Applications
Intended for patients indicated for an implantable cardioverter defibrillator per physician assessment.
Used in the management of life-threatening ventricular tachyarrhythmias.
Suitable for care pathways where avoidance of transvenous lead placement is a clinical consideration, as determined by the implanting physician.
Specific indications, contraindications, warnings, and precautions: refer to the official Medtronic Instructions for Use.

Product Information
Brand: Medtronic
Model / Family: Aurora EV-ICD MRI SureScan
REF / UPN: DVEA3E4
Category: ICD Devices | Implantable Cardioverter Defibrillators
Device Type: Extravascular implantable cardioverter defibrillator (EV-ICD)
MRI Status: MRI SureScan (conditional, per manufacturer labeling)
Remote Monitoring: Compatible with Medtronic CareLink (per manufacturer labeling)
Compatible Lead: Medtronic extravascular (substernal) defibrillation lead per IFU
Dimensions / Weight / Battery Longevity: Not specified in the located sources
Sterility / Single Use: Not specified in the located sources
Regulatory Status: Refer to official Medtronic documentation for the destination market

REF / UPNDVEA3E4
Size

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