BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Follow-up Information for Corrective Action for UniCel DxC systems, Beckman Coulter

Product group In-vitro diagnostics
Reference 00256/10

Follow-up Information for Corrective Action of Beckman Coulter for UniCel DxC 600, UniCel DxC 600 PRO, UniCel DxC 600i, UniCel DxC 800, Unicel DxC 800 PRO, UniCel DxC 880i, UniCel DxC 860i, UniCel DxC 680i, UniCel DxC 660i, because excessive build up of protein, bacteria and sample tube additives in the ISE flow cell may cause erroneous results. The customers were informed about the problem and how to avoid it.
(FSN in English is not available)

Follow-up Information for Corrective Action for UniCel DxC systems, Beckman Coulter , Download_VeroeffentlichtAm_EN PDF, 142KB, 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