
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 Abbott Fortify Assura DR Dual-Chamber ICD (REF CD2359-40) is an implantable cardioverter defibrillator designed to provide tachyarrhythmia detection, antitachycardia pacing, cardioversion, and defibrillation therapy together with dual-chamber bradycardia pacing. Engineered with Abbott's proven high-voltage platform, the Fortify Assura DR supports atrial and ventricular sensing for enhanced discrimination of supraventricular from ventricular arrhythmias.
Key Features
Dual-chamber ICD architecture with atrial and ventricular sensing and pacing channels
High-voltage defibrillation therapy for ventricular tachycardia and ventricular fibrillation
Antitachycardia pacing (ATP) options including burst and ramp protocols
SVT discrimination algorithms to help reduce inappropriate shocks
DF-1/IS-1 lead connector compatibility (verify against current Abbott technical manual)
Programmable bradycardia pacing modes including DDD, DDDR, and related dual-chamber modes
Diagnostic data storage including stored electrograms and arrhythmia episode logs
Compatible with Abbott Merlin programmer and Merlin.net remote monitoring (confirm with current Abbott documentation)
Clinical Applications
Intended for use in patients indicated for an implantable cardioverter defibrillator with dual-chamber pacing requirements
Management of life-threatening ventricular tachyarrhythmias
Patients requiring concurrent atrial sensing or pacing alongside ICD therapy
Long-term ambulatory cardiac rhythm monitoring through remote follow-up workflows
Product Information
Brand: Abbott (formerly St. Jude Medical)
Model Family: Fortify Assura DR
REF / UPN: CD2359-40
Device Type: Dual-Chamber Implantable Cardioverter Defibrillator (ICD)
Category: ICD Devices | Implantable Cardioverter Defibrillators
Connector Configuration: Not specified in the located sources
Dimensions and Weight: Not specified in the located sources
Battery Longevity: Not specified in the located sources
Packaging: Sterile, single-use device; verify shelf life and sterilization method on current product labeling
Regulatory Status: Refer to Abbott's current Instructions for Use and regional regulatory documentation prior to procurement
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