BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Corrective action for the Phadia 1000 instrument, Phadia AB

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 08022/14

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

Corrective action for the Phadia 1000 instrument, Phadia AB , Download_VeroeffentlichtAm_EN PDF, 153KB, File does not meet accessibility standards