IMMULITE®/IMMULITE® 1000 Systems SUBS X2 - SFDA Registration ME0000001481SFDAA00838
Access comprehensive regulatory information for IMMULITE®/IMMULITE® 1000 Systems SUBS X2 in the Saudi Arabia medical device market through Pure Global AI's free database. This General IVD(Others) device is registered with Saudi Arabia SFDA under registration number ME0000001481SFDAA00838 and manufactured by Siemens Healthcare diagnostics products Limited.
This page provides complete registration details including product category (Chemicals), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
Light emission which reacts with enzyme bound to the bead and is detected by a photomultiplier tube.
For use with the IMMULITE and IMMULITE 1000 Systems. Follow instructions in the IMMULITE or IMMULITE 1000 Operator's Manual.
[]