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 Evera MRI ICD (REF DVMB1D4) is a single-chamber implantable cardioverter defibrillator engineered to deliver life-saving tachyarrhythmia therapy while supporting patient access to MRI scanning under approved MR-conditional labeling. Its contoured PhysioCurve design, SmartShock detection algorithms and extended longevity platform make it a proven choice for ventricular tachycardia and ventricular fibrillation management.
Key Features
Single-chamber VVI/VVIR ICD platform with MRI SureScan technology for MR-conditional use when implanted as a complete SureScan system.
PhysioCurve ergonomic shape intended to improve patient comfort and reduce skin pressure.
SmartShock 2.0 discrimination algorithms designed to reduce inappropriate shocks.
ATP During Charging and tiered anti-tachycardia pacing therapies.
OptiVol fluid status monitoring and Cardiac Compass trends for remote patient management.
CareLink remote monitoring compatibility via wireless telemetry.
Extended battery longevity platform for reduced replacement frequency.
Clinical Applications
Primary and secondary prevention of sudden cardiac death in adult patients at risk of life-threatening ventricular tachyarrhythmias, as determined by the implanting physician in accordance with current guidelines and the device IFU.
Detection and therapy of ventricular tachycardia (VT) and ventricular fibrillation (VF) through tiered ATP and defibrillation therapy.
Continuous arrhythmia monitoring and diagnostic data collection to support longitudinal cardiac device follow-up.
Product Information
Brand: Medtronic
Model Family: Evera MRI
REF / UPN: DVMB1D4
Category: Implantable Cardioverter Defibrillators (ICD)
Chamber Configuration: Single-chamber (VR)
MRI Compatibility: MR-Conditional when implanted as a complete Medtronic SureScan system per IFU
Connector: Not specified in the located sources
Dimensions / Weight / Volume: Not specified in the located sources
Projected Longevity: Not specified in the located sources
Sterility: Supplied sterile for single use; verify sterility and expiration prior to implantation
Storage: Store per manufacturer IFU
Always consult the current Medtronic Evera MRI IFU and regional regulatory labeling before clinical use or procurement decisions.
REF / UPNDVMB1D4
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