REFLOTRON URIC ACID - SFDA Registration ME0000000652SFDAA00013
Access comprehensive regulatory information for REFLOTRON URIC ACID 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 ME0000000652SFDAA00013 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.
uric acid quantitative determination Test
Test for the quantitative determination of uric acid in blood, serum or plasma with Reflotron.
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