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 Visia AF MRI / Visia AF ICD (REF DVAB1D1) is a single-chamber implantable cardioverter defibrillator engineered to deliver tachyarrhythmia therapy while providing dedicated atrial fibrillation (AF) detection capabilities from a single ventricular lead system. As part of Medtronic's SureScan portfolio, the device is designed to support patient access to MRI scanning under specified conditions of use, and integrates established Medtronic detection and therapy algorithms intended to reduce inappropriate shocks.
Key Features
- Single-chamber ICD platform with integrated AF detection from the ventricular lead
- SureScan design intended for MR Conditional labeling when implanted as a complete SureScan system
- SmartShock discrimination algorithms to help reduce inappropriate therapy
- OptiVol and Cardiac Compass trending tools for long-term patient management (availability per device configuration; confirm in IFU)
- CareLink remote monitoring compatibility
- Programmable tachyarrhythmia detection zones with ATP (Anti-Tachycardia Pacing) and high-energy defibrillation therapy
- Compact titanium housing for pectoral implantation
Clinical Applications
- Single-chamber ICD therapy for patients indicated for prevention of sudden cardiac death
- Detection and monitoring of atrial fibrillation episodes via ventricular-based algorithms
- Delivery of ATP and defibrillation therapy for ventricular tachycardia and ventricular fibrillation
- Long-term arrhythmia diagnostics and remote follow-up workflows
- Use in patients who may require access to MRI scanning under SureScan conditions of use
Product Information
- Brand: Medtronic
- Model: Visia AF MRI / Visia AF
- REF / UPN: DVAB1D1
- Category: Implantable Cardioverter Defibrillators (ICD)
- Configuration: Single-chamber ICD
- MRI Status: MR Conditional under SureScan system labeling (refer to current IFU and MRI technical manual for scan conditions)
- Connector: DF4/IS-1 compatible per platform specification — confirm in official Medtronic product specification
- Remote Monitoring: Medtronic CareLink compatible
- Sterility / Packaging / Shelf Life: Not specified in the located sources — verify on packaging label
- Battery longevity, dimensions and mass: Not specified in the located sources — refer to official Medtronic device specification sheet
- Regulatory status and clinical suitability: Refer to local regulatory labeling and the official Instructions for Use prior to procurement or implantation
REF / UPNDVAB1D1
Size
Medtronic Visia AF MRIVisia AF ICDDVAB1D1Medtronic ICDsingle chamber ICDimplantable cardioverter defibrillatorAF detection ICDSureScan MRI ICDMR conditional defibrillatorSmartShock ICDCareLink remote monitoringMedtronic defibrillator suppliercardiac rhythm management deviceICD procurementB2B medical device sourcing
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