BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall of LAA Occluder, Occlutech International AB

Product group Non-active implants - cardiac surgery
Reference 08384/16

For further information as well as details concerning the device please see the enclosed Advisory Notice of the manufacturer.

Recall of LAA Occluder, Occlutech International AB , Download_VeroeffentlichtAm_EN PDF, 190KB, File does not meet accessibility standards