Medtronic Evera MRI ICD | REF DDMB1D1

The Medtronic Evera MRI ICD (REF DDMB1D1) is a single-chamber implantable cardioverter defibrillator from the Evera MRI SureScan family, engineered to deliver automatic detection and therapy for life-threatening ventricular tachyarrhythmias while enabling patients to undergo MRI scanning under specified conditions. The device features a physiologically contoured PhysioCurve design intended to improve patient comfort and reduce skin pressure at the implant pocket, together with SmartShock 2.0 discrimination algorithms aimed at reducing inappropriate shocks.

Key Features
- MRI SureScan technology for MR Conditional scanning when implanted as a complete SureScan system
- Single-chamber VVE-VVIR ICD configuration with defibrillation, cardioversion and anti-tachycardia pacing (ATP) therapies
- SmartShock 2.0 algorithms including Wavelet, Onset, Stability, RV Lead Noise Discrimination, T-Wave Discrimination and Confirmation+
- PhysioCurve contoured shape for anatomic fit
- OptiVol 2.0 fluid status monitoring and Cardiac Compass trends
- Wireless CareLink remote monitoring compatibility
- Extended longevity battery design
- Connector configuration: DF-1 / IS-1 (confirm against implant documentation)

Clinical Applications
- Primary and secondary prevention of sudden cardiac death in indicated patient populations
- Treatment of ventricular tachycardia (VT) and ventricular fibrillation (VF) via ATP, cardioversion and defibrillation
- Bradycardia support pacing in the right ventricle
- Long-term rhythm surveillance and remote follow-up in cardiology and electrophysiology programs
- Use in patients who may require MRI diagnostic imaging under MR Conditional scanning conditions

Product Information
Brand: Medtronic
Product Line: Evera MRI SureScan ICD
REF / UPN: DDMB1D1
Category: Implantable Cardioverter Defibrillators (ICD)
Chamber Configuration: Single-chamber (VR)
MRI Compatibility: MR Conditional when implanted as a complete Medtronic SureScan system and scanned per IFU conditions
Connector: DF-1 / IS-1 (verify with device IFU)
Sterility: Supplied sterile, single use
Storage: Store per manufacturer IFU
Regulatory Status: Not specified in the located sources; buyers must verify local regulatory clearance
Clinical Use: Implantation, programming and follow-up to be performed only by qualified physicians in accordance with the Medtronic Instructions for Use

REF / UPNDDMB1D1
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