BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall of one lot of the Dilatator, De Bakey, Gebrüder Martin GmbH

Product group Medical instruments for use in humans - vascular surgery
Reference 01118/13

The manufacturer Gebrüder Martin GmbH informs about the recall of one lot of the Dilatator, De Bakey, because the solded tube of the dilatator may drop off at the end of the procedure.

Recall of one lot of the Dilatator, De Bakey, Gebrüder Martin GmbH , Download_VeroeffentlichtAm_EN PDF, 211KB, 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