ELISA reagent kits for determining the concentration of sex hormones in the composition (see appendix) Cobas Core Testosterone EIA; Cobas Core Estradiol EIA - Cobas Core Estradiol EIA; Cobas Core Progesterone EIA - Cobas Core Progesterone EIA; Kobas Kore Steroid Diluent... (see the full description in the card) - Roszdravnadzor Registration МЗ РФ № 2001/381

Access comprehensive regulatory information for ELISA reagent kits for determining the concentration of sex hormones in the composition (see appendix) Cobas Core Testosterone EIA; Cobas Core Estradiol EIA - Cobas Core Estradiol EIA; Cobas Core Progesterone EIA - Cobas Core Progesterone EIA; Kobas Kore Steroid Diluent... (see the full description in the card) in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number МЗ РФ № 2001/381 and manufactured by F.Hoffmann-La Roche Ltd./ Roche Diagnostics GmbH. The device was registered on April 11, 2001.

This page provides complete registration details including device type, manufacturer information, country of origin (Switzerland;Germany), 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.