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This webpage is a global product listing of Medtronic, MR-conditional implantable cardiac devices, including pacemakers, ICDs, CRTs, and ICMs. It is intended to assist healthcare professionals in determining if an implanted system is MR Conditional.
This webpage is a global search tool of Medtronic, MR-conditional implantable cardiac devices, including pacemakers, ICDs, CRTs, and ICMs. It is intended to assist healthcare professionals in determining if an implanted system is MR Conditional.
Medtronic MRI Verify allows you to look up the MR conditionality of a patient’s Medtronic cardiac implantable electronic device based on the information available.
Advisa™ MRI pacemaker. The Advisa™ MRI SureScan™ pacemaker is the second-generation pacing system approved by the FDA designed for safe use in the MRI environment when specific conditions are met. Advisa is available in single and dual chamber options. Model numbers: A2DR01, A3SR01.
Present your device identification card to your doctor to inform the physician that you have a complete heart device system that may allow you access to an MRI scan. Your identification card will help your physician understand what kind of implantable device you have.
Medtronic SureScan systems are MR Conditional, and as such are designed to allow patients to undergo MRI under the specified conditions for use. Micra, Reveal LINQ, and transvenous SureScan system patients may be scanned using a horizontal field, cylindrical bore, clinical 1.5T or 3T MRI system for hydrogen proton imaging. When programmed to
MRI can put pacemaker patients at risk. We believe patient MRI safety must be proven by rigorous scientific testing and regulatory review. Micra AV2 and Micra VR2 leadless pacemakers are FDA approved for ≤ 3T, including low-field, MRI scans.
