Reagent kit for determining the activity of alkaline phosphatase in serum and blood plasma by the endpoint method (ALKALINE PHOSPHATASE-2-OLVEX) according to TU 9398-047-44276594-2009 - Roszdravnadzor Registration ФСР 2009/05991

Access comprehensive regulatory information for Reagent kit for determining the activity of alkaline phosphatase in serum and blood plasma by the endpoint method (ALKALINE PHOSPHATASE-2-OLVEX) according to TU 9398-047-44276594-2009 in the Russia medical device market through Pure Global AI's free database. This Class 2a medical device is registered under Roszdravnadzor registration number ФСР 2009/05991 and manufactured by OLVEX DIAGNOSTICS LLC. The device was registered on December 28, 2022.

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.