ADVIA 120, ADVIA 2120, ADVIA 2120i PEROX SHEATH - SFDA Registration ME0000004050SFDAA00034

Access comprehensive regulatory information for ADVIA 120, ADVIA 2120, ADVIA 2120i PEROX SHEATH 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 ME0000004050SFDAA00034 and manufactured by Siemens Healthcare Diagnostics Inc..

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.