
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 DDMC3D1) is a dual-chamber implantable cardioverter defibrillator from Medtronic's Evera MRI SureScan family. Designed with a physiologically shaped PhysioCurve design intended to improve patient comfort, the device delivers tachyarrhythmia detection and therapy while offering MR Conditional labeling that supports access to MRI scanning when conditions of use are followed.
Key Features
- MR Conditional design (SureScan technology) intended to allow MRI scanning under specified conditions
- Dual-chamber ICD configuration for atrial and ventricular sensing, pacing, and defibrillation therapy
- PhysioCurve contoured shape engineered for implant comfort
- SmartShock 2.0 detection algorithms intended to help reduce inappropriate shocks
- Extended longevity battery chemistry typical of the Evera MRI platform
- Wireless CareLink remote monitoring compatibility
- Programmable bradycardia, anti-tachycardia pacing (ATP), cardioversion and defibrillation therapies
Clinical Applications
- Intended for patients indicated for an implantable cardioverter defibrillator for the treatment of life-threatening ventricular tachyarrhythmias
- Supports management of bradyarrhythmias requiring dual-chamber pacing
- Suitable for patient populations where future MRI access may be a clinical consideration, subject to MR Conditional labeling
- Remote follow-up workflows via the Medtronic CareLink Network
Product Information
- Brand: Medtronic
- Product Family: Evera MRI SureScan ICD
- Category: ICD Devices | Implantable Cardioverter Defibrillators
- Configuration: Dual-chamber ICD
- REF / UPN: DDMC3D1
- MRI Status: MR Conditional (refer to current manufacturer MRI technical guide for conditions of use)
- Connector Type: Not specified in the located sources
- Dimensions / Weight / Volume: Not specified in the located sources
- Sterility / Shelf Life: Refer to product labeling
- Regulatory Status: Refer to manufacturer documentation for region-specific approvals
- Important: For use by qualified healthcare professionals; consult the current Medtronic Instructions for Use (IFU) and MRI technical manual prior to implant or scanning.
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