BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Urgent Safety Notice/Corrective action for Terumo® Radifocus Guide Wire M, Terumo Europe NV

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 02814/15

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

Urgent Safety Notice/Corrective action for Terumo® Radifocus Guide Wire M, Terumo Europe NV , Download_VeroeffentlichtAm_EN PDF, 104KB, 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