REFLOTRON* UREA - SFDA Registration ME0000000652SFDAA00012

Access comprehensive regulatory information for REFLOTRON* UREA 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 ME0000000652SFDAA00012 and manufactured by Roche Diagnostics GmbH.

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.