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 ICD (REF DVFC3D4) is a single-chamber implantable cardioverter defibrillator engineered to deliver ventricular tachyarrhythmia therapy while providing diagnostic insight into atrial fibrillation through a single right-ventricular lead. Part of Medtronic's SureScan portfolio, the Visia AF MRI is designed with MR Conditional labeling to support patient access to magnetic resonance imaging when scanned under specified conditions. This listing is intended for qualified hospital procurement, distributor, and clinical engineering buyers sourcing genuine Medtronic ICD inventory.
Key Features
- AF detection without an atrial lead: Proprietary algorithms infer atrial fibrillation episodes from a single ventricular lead, supporting AF burden monitoring in single-chamber patients.
- MRI SureScan technology: MR Conditional system labeling intended to allow full-body MRI scanning under Medtronic-defined conditions of use.
- SmartShock 2.0 discrimination: Designed to reduce inappropriate shocks by differentiating ventricular from supraventricular arrhythmias and identifying lead noise.
- OptiVol fluid status monitoring: Trends thoracic impedance to support heart-failure management workflows.
- CareLink remote monitoring compatibility: Supports scheduled and alert-based wireless follow-up via the Medtronic CareLink Network.
- Single-chamber VR configuration: DF-1/IS-1 connector configuration consistent with the DVFC3D4 model designation; refer to the IFU for definitive header port details.
- Longevity-oriented design: Power management features intended to extend projected service life under nominal programming.
Clinical Applications
- Primary and secondary prevention of sudden cardiac death in indicated single-chamber ICD candidates.
- Patients with documented or suspected paroxysmal atrial fibrillation where AF burden quantification is clinically valuable.
- Cases requiring future MRI access under MR Conditional scanning protocols.
- Heart-failure populations benefiting from impedance-based fluid trend data.
- Remote follow-up programs leveraging CareLink for episode review and device diagnostics.
Product Information
- Manufacturer: Medtronic
- Product family: Visia AF MRI / Visia AF ICD
- Model / REF: DVFC3D4
- Category: Implantable Cardioverter Defibrillator (ICD)
- Chamber configuration: Single-chamber (VR)
- MRI labeling: MR Conditional (SureScan) under Medtronic-specified conditions
- Connector configuration: Not specified in the located sources; verify against current Medtronic IFU
- Device dimensions and mass: Not specified in the located sources
- Projected longevity: Not specified in the located sources
- Sterility: Supplied sterile for single use; do not resterilize
- Regulatory status: Refer to the Medtronic Instructions for Use and local regulatory documentation for market-specific approvals and indications.
REF / UPNDVFC3D4
Size
Medtronic Visia AF MRIVisia AF ICDDVFC3D4Medtronic ICDsingle chamber ICDimplantable cardioverter defibrillatorMRI conditional ICDSureScan ICDSmartShock 2.0OptiVol fluid monitoringatrial fibrillation detectionCareLink remote monitoringcardiac rhythm managementsudden cardiac death preventionB2B medical device procurement
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