
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 EMBLEM Subcutaneous S-ICD Device (REF A219) is an implantable cardioverter defibrillator engineered to deliver defibrillation therapy through a subcutaneous lead, leaving the heart and vasculature untouched. The EMBLEM platform is positioned as an alternative to transvenous ICD systems for selected patients who require protection from sudden cardiac arrest.
As part of Boston Scientific's S-ICD portfolio, the device is intended for use with a compatible subcutaneous electrode and the manufacturer's programming and patient management ecosystem.
Key Features
Subcutaneous design with no transvenous or epicardial leads required.
Delivers defibrillation therapy for ventricular tachyarrhythmias.
Compatible with Boston Scientific's subcutaneous electrode and programmer system.
Engineered for long-term implant performance; battery longevity per manufacturer specifications.
Supports remote patient monitoring through the manufacturer's patient management network.
SMART Pass and SMART Charge algorithms intended to support arrhythmia discrimination (per manufacturer literature).
Clinical Applications
Intended to provide defibrillation therapy in patients at risk of life-threatening ventricular tachyarrhythmias where a subcutaneous approach is appropriate.
Considered for patients with limited venous access, prior device infection, or other clinical reasons to avoid transvenous leads.
Use, indications, contraindications, warnings, and precautions are defined in the manufacturer's Instructions for Use (IFU).
Product Information
Brand: Boston Scientific
Product Family: EMBLEM Subcutaneous S-ICD
REF / UPN: A219
Category: ICD Devices | Implantable Cardioverter Defibrillators
Device Type: Subcutaneous Implantable Cardioverter Defibrillator (S-ICD)
Lead Compatibility: Boston Scientific subcutaneous electrode (refer to manufacturer compatibility matrix)
Dimensions / Weight / Battery Longevity: Not specified in the located sources
MRI Conditional Status: Not specified in the located sources; refer to current manufacturer IFU
Sterility / Single Use: Refer to manufacturer labeling
Regulatory Status: Refer to manufacturer documentation for the destination market
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