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 DVFB1D4) is a single-chamber implantable cardioverter defibrillator engineered to deliver high-energy defibrillation therapy together with proprietary atrial fibrillation (AF) detection capability in a single-lead system. Designed for the management of life-threatening ventricular tachyarrhythmias, the device integrates Medtronic's PR Logic and Wavelet discrimination algorithms with AF detection diagnostics typically reserved for dual-chamber platforms, supporting clinicians in arrhythmia characterization while maintaining the simplicity of a single-chamber implant.
Key Features
- Single-chamber ICD platform with high-voltage defibrillation therapy
- AF detection diagnostics from a single ventricular lead
- SmartShock 2.0 technology to help reduce inappropriate shocks
- PR Logic and Wavelet SVT/VT discrimination algorithms
- MRI SureScan technology supporting MRI conditional scanning under specified conditions
- OptiVol fluid status monitoring (per labeled configuration)
- CareLink remote monitoring compatibility
- Programmable bradycardia pacing modes
Clinical Applications
- Primary and secondary prevention of sudden cardiac death in indicated patients
- Detection and termination of ventricular tachycardia and ventricular fibrillation
- Single-chamber ICD therapy where AF burden monitoring is clinically relevant
- Long-term remote follow-up via Medtronic CareLink Network
- Patient populations requiring MRI access under conditional scanning protocols
Product Information
- Brand: Medtronic
- Model Family: Visia AF MRI / Visia AF
- REF / UPN: DVFB1D4
- Category: Implantable Cardioverter Defibrillators (ICD)
- Configuration: Single-chamber ICD
- MRI Compatibility: MR Conditional under labeled SureScan conditions (refer to manufacturer IFU)
- Connector: Not specified in the located sources
- Battery Longevity: Not specified in the located sources
- Device Dimensions / Mass: Not specified in the located sources
- Storage: Refer to manufacturer instructions for use
- Use: Sterile, single-use implantable device. Implantation and programming must be performed by qualified cardiac electrophysiology professionals in accordance with the official Medtronic IFU.
REF / UPNDVFB1D4
Size
Medtronic Visia AF MRIVisia AF ICDDVFB1D4Medtronic ICDsingle chamber ICDimplantable cardioverter defibrillatorMRI conditional ICDSureScan ICDSmartShock 2.0atrial fibrillation detection ICDPR Logic algorithmCareLink remote monitoringcardiac rhythm management devicesudden cardiac death preventionB2B medical device procurement
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