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CAIRE Reporting, LLC Launches the First Comprehensive Adverse Incident Reporting Web Portal for Magnetic Resonance Imaging

CAIRE Reporting, LLC Launches the First Comprehensive Adverse Incident Reporting Web Portal for Magnetic Resonance Imaging
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Update on Electronic Exam Administration Announced by American Board of Magnetic Resonance Safety

The American Board of Magnetic Resonance Safety (ABMRS) recently announced an update on its electronic exam administration. Beginning this summer, the ABMRS will offer their credentialing exams for MR Medical Director (MRMD), MR Safety Officer (MRSO) and MR Safety Expert (MRSE) at testing centers operated by Prometric, LLC.

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Medtronic Receives FDA Approval for Expanded MRI Labeling of InterStim™ SureScan™ MRI Leads

Medtronic Receives FDA Approval for Expanded MRI Labeling of InterStim™ SureScan™ MRI Leads News provided by Share this article Share this article DUBLIN, Feb. 18, 2021 /PRNewswire/ -- Medtronic plc (NYSE:MDT), the global leader in medical technology, today announced it has received approval from the United States Food and Drug Administration (FDA) for expanded MRI labeling of its InterStim™ II and InterStim™ Micro sacral neuromodulation (SNM) systems that use SureScan™ MRI leads. The updated MRI Guidelines allow for a wider range of MRI scan parameters and shorter wait time between MRI scans, thereby improving patient access to MRI exams and adding flexibility for MRI providers. It applies to existing and future implants of InterStim systems that use SureScan MRI leads.

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