
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 DDMD3D1) is a single-chamber implantable cardioverter defibrillator from Medtronic's Primo MRI SureScan platform. Designed for procurement by hospitals, electrophysiology labs and cardiac care facilities, this device combines defibrillation therapy with MRI conditional design intended to support patients who may require diagnostic magnetic resonance imaging during the lifetime of the device.
Key Features
MRI SureScan technology engineered for use under specified MRI scanning conditions.
Single-chamber ICD configuration for ventricular sensing, pacing and defibrillation therapy.
SmartShock detection algorithms designed to help discriminate appropriate from inappropriate therapy.
Compact titanium can suitable for pectoral implantation.
Compatible with Medtronic CareLink remote monitoring ecosystem.
Programmable tachyarrhythmia detection and therapy parameters.
Bradycardia pacing support with rate-responsive options.
Battery longevity profile optimized for extended service life under typical programming.
Clinical Applications
Cardiac rhythm management for patients indicated for ICD therapy.
Treatment programs addressing ventricular tachyarrhythmias, including ventricular tachycardia and ventricular fibrillation.
Primary and secondary prevention of sudden cardiac arrest within accepted clinical guidelines.
Patient pathways where future MRI imaging access may be a procurement consideration.
Electrophysiology and cardiology service lines requiring single-chamber defibrillation devices.
Product Information
Brand: Medtronic
Model / Family: Primo MRI ICD (SureScan)
REF / UPN: DDMD3D1
Category: Implantable Cardioverter Defibrillators (ICD)
Configuration: Single-chamber ICD
MRI Status: MRI Conditional under manufacturer-specified scanning conditions
Connector Standard: Not specified in the located sources
Device Dimensions / Mass / Volume: Not specified in the located sources
Battery Longevity: Not specified in the located sources
Sterility: Supplied sterile for single use; refer to manufacturer IFU
Storage and Handling: Per Medtronic instructions for use
Regulatory Status: Refer to local Medtronic representative for region-specific clearance and availability
Buyers should always confirm current specifications, lead configuration compatibility, MRI conditions of use and regulatory status with official Medtronic documentation and the product's Instructions for Use prior to procurement.
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