
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 HF ICD (REF D532) is an implantable cardioverter defibrillator engineered to deliver tachyarrhythmia detection and therapy with integrated heart failure diagnostic tools. As part of the RESONATE family, the device is designed to support clinicians in long-term management of patients at risk of life-threatening ventricular arrhythmias while providing trended physiologic data to inform follow-up decisions.
Key Features
Single-chamber ICD platform under the RESONATE family from Boston Scientific.
HeartLogic-class heart failure diagnostic capability for trended patient status monitoring.
Tachyarrhythmia detection with antitachycardia pacing (ATP) and high-energy defibrillation therapy.
RF wireless telemetry compatible with the LATITUDE remote patient management ecosystem.
MRI conditional labeling under the ImageReady program — verify conditions in the current IFU.
Longevity and physical dimensions: Not specified in the located sources.
Clinical Applications
Intended for use in patients indicated for an implantable cardioverter defibrillator for the treatment of ventricular tachyarrhythmias.
Supports clinician workflows for primary and secondary prevention of sudden cardiac death per device labeling.
Provides heart failure trend data that may assist in patient follow-up and care planning.
Compatible with remote monitoring strategies for ambulatory cardiac device patients.
Product Information
Brand: Boston Scientific
Product Line: RESONATE HF ICD
REF / UPN: D532
Category: ICD Devices | Implantable Cardioverter Defibrillators
Connector / Lead Configuration: Not specified in the located sources
Sterility & Single Use: Supplied sterile for single-patient implant per manufacturer labeling — confirm in current IFU.
Regulatory Status: Refer to the official Boston Scientific IFU and regional regulatory documentation.
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