BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Safety Corrective Action regarding Eon Mini model 65-3788 and Brio model 65-6788, St. Jude Medical

2012.08.03

Product group Active implantable medical devices - biostimulators
Reference 04939/12

St. Jude Medical has issued a Field Safety Corrective Action regarding the implantable electrical stimulation systems Eon Mini model 65-3788 and Brio model 65-6788.

Safety Corrective Action regarding Eon Mini model 65-3788 and Brio model 65-6788, St. Jude Medical , Download_VeroeffentlichtAm_EN PDF, 74KB, File does not meet accessibility standards

Use of cookies

Cookies help us to provide our services. By using our website you agree that we can use cookies. Read more about our Privacy Policy and visit the following link: Privacy Policy (only in German)

OK