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SureScan™ implantable cardiac devices

Unmatched MRI access

Annually, 12–16% of device patients are likely to have an MRI ordered.^1–4 Historically, less than 1% would have received a scan.^1–4 Today, with our exclusive MRI portfolio, you can ensure safe MRI access for most patients when MR conditions are met.

Medtronic has long been committed to providing cardiac device patients with access to the diagnostic and treatment benefits of MRI. Our portfolio of SureScan™ cardiac resynchronization therapy pacemaker (CRT-P), cardiac resynchronization therapy defibrillator (CRT-D), implantable cardioverter defibrillator (ICD), pacemakers (IPG), and insertable cardiac monitor (ICM) systems provides exactly that — safe, full body MRI access.

No MRI exclusion zone
SureScan™ devices and leads that work in any combination
1.5T and 3T full body MRI scanning across the portfolio^†

MR Conditional product search

View all components of a SureScan™ system by using our comprehensive product search tool.

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† Revo MRI™ pacemaker is only labeled 1.5T MR Conditional.

Based on data from 2010 MarketScan® Commercial and Medicare databases from Truven Health Analytics, Inc. Data used to characterize non-pacemaker and pacemaker cohorts and utilization or radiology services. Cohorts were matched based on age, gender, and comorbidities.
Based on ICD data from MarketScan® 2012 Commercial and Medicare Database, Truven Health Analytics. 2015 Medtronic data on file.
Nazarian S, Reynolds MR, Ryan MP, et al. Utilization and likelihood of radiologic diagnostic imaging in patients with implantable cardiac defibrillators. J Magn Reson Imaging. 2016;43(1):115–127.
Based on CRT data from MarketScan® 2012 Commercial and Medicare Database, Truven Health Analytics. 1015 Medtronic data on file.

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