BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Urgent Safety Notice for the Omnis system, Dako Denmark A/S

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 02341/15

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

Urgent Safety Notice for the Omnis system, Dako Denmark A/S , Download_VeroeffentlichtAm_EN PDF, 225KB, File does not meet accessibility standards