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 Medtronic Primo MRI ICD (REF DDMD3D4) is a dual-chamber implantable cardioverter defibrillator designed to deliver high-voltage therapy for life-threatening ventricular tachyarrhythmias while providing dual-chamber bradycardia pacing support. Built on Medtronic's SureScan platform, the device is engineered to allow patients access to MRI scanning under specified conditions of use, helping clinicians balance long-term arrhythmia management with future diagnostic imaging needs.
Key Features
Dual-chamber ICD configuration with atrial and ventricular sensing, pacing and defibrillation capabilities.
SureScan MRI-conditional design intended to allow MRI scanning when device-specific conditions of use are met.
Medtronic detection and discrimination algorithms designed to help differentiate supraventricular from ventricular tachyarrhythmias.
High-voltage therapy delivery for cardioversion and defibrillation of ventricular tachycardia and ventricular fibrillation.
Anti-tachycardia pacing (ATP) options intended to terminate ventricular tachycardia prior to shock delivery.
Programmable bradycardia pacing modes for atrial and ventricular support.
OptiVol and Cardiac Compass style diagnostic trends to support remote follow-up workflows (consult IFU for model-specific availability).
CareLink remote monitoring compatibility for longitudinal device and patient data review.
Titanium-encased pulse generator designed for chronic implantation.
DF4/IS-1 lead connector configuration — verify against the official product specification sheet prior to ordering.
Clinical Applications
Primary and secondary prevention of sudden cardiac death in patients meeting implant criteria as determined by the treating physician.
Management of documented ventricular tachycardia and ventricular fibrillation.
Dual-chamber pacing support for patients with concomitant bradyarrhythmia indications.
Long-term rhythm surveillance and arrhythmia diagnostics in cardiology and electrophysiology programs.
Patient populations who may require future MRI examinations under labeled conditions of use.
Product Information
Brand: Medtronic
Product: Primo MRI ICD
REF / UPN: DDMD3D4
Category: ICD Devices | Implantable Cardioverter Defibrillators
Device Type: Dual-chamber implantable cardioverter defibrillator
MRI Status: MRI-conditional under Medtronic SureScan labeled conditions of use
Lead Connector: Not specified in the located sources — confirm via official Medtronic product specification sheet
Longevity / Battery: Not specified in the located sources
Dimensions / Mass: Not specified in the located sources
Remote Monitoring: Compatible with Medtronic CareLink Network
Sterility: Supplied sterile for single use; do not resterilize
Storage: Store per manufacturer Instructions for Use
Regulatory: Refer to current Medtronic IFU and regional regulatory documentation for approved indications and conditions of use.
REF / UPNDDMD3D4
Size
Medtronic Primo MRI ICDREF DDMD3D4Medtronic ICDdual chamber ICDimplantable cardioverter defibrillatorMRI conditional ICDSureScan ICDcardiac rhythm management deviceventricular tachyarrhythmia therapyanti-tachycardia pacing devicesudden cardiac death preventionCareLink remote monitoring ICDelectrophysiology implantable devicecardiology ICD supplierB2B medical device procurement
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