
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 Boston Scientific RESONATE ICD (REF D433) is an implantable cardioverter defibrillator designed to deliver high-voltage therapy for the treatment of ventricular tachyarrhythmias. Part of the RESONATE platform, the device integrates advanced diagnostics and remote monitoring features intended to support long-term patient management in hospital and outpatient cardiology settings.
Key Features
- HeartLogic Heart Failure Diagnostic designed to provide early indication of worsening heart failure by combining multiple physiologic sensors
- High-voltage defibrillation therapy with programmable shock and anti-tachycardia pacing (ATP) options
- RF telemetry compatibility with the LATITUDE NXT Remote Patient Management system
- MRI conditional labeling as specified by the manufacturer's ImageReady documentation
- Extended projected longevity supported by battery and circuitry design
- Compact titanium housing intended for pectoral implantation
Clinical Applications
- Detection and termination of ventricular tachycardia (VT) and ventricular fibrillation (VF)
- Secondary prevention of sudden cardiac death in patients meeting implant criteria
- Primary prevention in patients at elevated risk of life-threatening ventricular arrhythmias
- Long-term arrhythmia monitoring and heart failure trend analysis via HeartLogic and remote follow-up
Product Information
Brand: Boston Scientific
Model/Family: RESONATE ICD
REF/UPN: D433
Category: ICD Devices | Implantable Cardioverter Defibrillators
Device Type: Implantable cardioverter defibrillator (single-chamber configuration typical of D433)
Connector Standard: Not specified in the located sources
Dimensions / Weight / Volume: Not specified in the located sources
Projected Longevity: Not specified in the located sources
Sterilization: Supplied sterile by the manufacturer; refer to IFU
Regulatory Status: Refer to manufacturer documentation for region-specific approvals
Condition: Please confirm with supplier at time of quotation
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