BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Corrective action for the products rHead, uHead, Sigmoid Notch, ReMotion, Radio Capitellum, Stryker Trauma AG - Division Trauma and Extremities

Product group Non-active implants - bone surgery
Reference 03689/15

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

Corrective action for the products rHead, uHead, Sigmoid Notch, ReMotion, Radio Capitellum, Stryker Trauma AG - Division Trauma and Extremities , Download_VeroeffentlichtAm_EN PDF, 422KB, 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)