A set of reagents for the quantitative determination of uric acid content by the enzymatic method in blood serum and urine (URIC ACID PS DDS) - Roszdravnadzor Registration ФС 012б3040/2825-06

Access comprehensive regulatory information for A set of reagents for the quantitative determination of uric acid content by the enzymatic method in blood serum and urine (URIC ACID PS DDS) in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number ФС 012б3040/2825-06 and manufactured by CJSC Diakon-DS. The device was registered on April 14, 2006.

This page provides complete registration details including device type, manufacturer information, country of origin (Russia), and regulatory compliance data from the official Russia Roszdravnadzor medical device database. Pure Global AI offers free access to Russia's complete medical device registry, helping global MedTech companies navigate Roszdravnadzor regulations efficiently.