BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Corrective action for the KODAK DirectView DR 7500 System, Carestream Health, Inc.

2014.07.29

Product group Radiological technology - stationary radiological equipment
Reference 03976/14

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

Corrective action for the KODAK DirectView DR 7500 System, Carestream Health, Inc. , Download_VeroeffentlichtAm_EN PDF, 21KB, 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