Biotronik’s single and dual-chamber pacemakers and Implantable Cardioverter Defibrillators (ICD) have gained European Commission (CE) approval for use in 3 Tesla (T) MRI scans worldwide
Biotronik's pacemakers and ICDs are part of their Pro-MRI range
Dr Maurizio Lunati, Niguarda Hospital, Milan, said: "3T scanners offer superior image quality, as well as a shorter scan time compared to a 1.5T machine.
“Patients with ProMRI devices enabling 3T scans benefit from a shorter time spent in the sometimes uncomfortable MRI machine, while doctors benefit from clearer images to diagnose conditions.
“Reduced scan times can improve clinical workflow, granting more patients access to this vital diagnostic tool."
To help physicians keep track of which ProMRI devices and leads are approved in their own region, new functions have been added to the ProMRI Systems Check website at www.promricheck.com.
ProMRI System Check allows physicians to verify whether a patient's individual Biotronik device and lead combination is MR conditional, and under which scanning conditions.
Manuel Ortega, senior vice president of Biotronik, said: "As 3T MRI scanners become more and more prevalent, it is essential that device patients are able to access them."
"Through innovation and diligence we have developed the world's largest portfolio of ProMRI devices.
“We are pleased to expand our existing portfolio of approved ICDs and pacemakers by gaining CE approval for 3T MRI scanning for the latest pacemaker generations."