
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 INOGEN ICD (REF D143) is an implantable cardioverter defibrillator engineered to provide automated detection and therapy for life-threatening ventricular tachyarrhythmias. Part of Boston Scientific's INOGEN family, this device combines defibrillation, cardioversion, antitachycardia pacing and bradycardia pacing support in a compact pulse generator intended for chronic implantation. This listing is provided for B2B procurement and catalog reference purposes only.
Key Features
Single-chamber implantable cardioverter defibrillator platform.
Automated detection of ventricular tachycardia (VT) and ventricular fibrillation (VF).
High-voltage shock therapy for cardioversion and defibrillation.
Antitachycardia pacing (ATP) for painless termination of VT episodes.
Bradycardia pacing support.
Diagnostic data storage including stored electrograms and episode logs.
Compatible with Boston Scientific LATITUDE remote patient management (model-specific configuration: Not specified in the located sources).
Programmer compatibility and telemetry options: Not specified in the located sources.
Clinical Applications
Intended for use in patients at risk of life-threatening ventricular tachyarrhythmias.
Secondary prevention in patients with prior sustained VT or VF episodes.
Primary prevention in patients meeting accepted clinical criteria for ICD therapy.
Management of recurrent symptomatic ventricular tachycardia requiring ATP or shock therapy.
Adjunctive bradycardia pacing where indicated.
Final clinical suitability must be determined by the implanting physician according to the official Instructions for Use and applicable guidelines.
Product Information
Brand: Boston Scientific
Product Family: INOGEN ICD
REF / UPN: D143
Category: ICD Devices | Implantable Cardioverter Defibrillators
Device Type: Implantable Cardioverter Defibrillator (Pulse Generator)
Configuration: Single-chamber (VR)
Lead Connector: Not specified in the located sources
Dimensions / Weight / Volume: Not specified in the located sources
Battery Chemistry and Longevity: Not specified in the located sources
MRI Conditional Status: Not specified in the located sources
Sterility: Supplied sterile for single use; verify packaging and expiry prior to implantation.
Storage: Store per manufacturer's labeling.
Regulatory: Refer to manufacturer documentation for region-specific regulatory status.
Note: Always consult the official Boston Scientific Instructions for Use (IFU) and product manual for complete specifications, warnings, contraindications, and programming details.
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