ELISA reagent kits for the determination of markers of TORCH infections in the composition (see appendix) Cobas Core Toxo IgG EIA; Kobas Kore Toho IgM ELISA Recomb. - Cobas Core Toxo IgM EIA recomb.; Kobas Kore Rubella IgG ELISA Recomb. - Cobas Core Rubella IgG EIA recomb.; Kobas Kor... (see the full description in the card) - Roszdravnadzor Registration МЗ РФ № 2001/389

Access comprehensive regulatory information for ELISA reagent kits for the determination of markers of TORCH infections in the composition (see appendix) Cobas Core Toxo IgG EIA; Kobas Kore Toho IgM ELISA Recomb. - Cobas Core Toxo IgM EIA recomb.; Kobas Kore Rubella IgG ELISA Recomb. - Cobas Core Rubella IgG EIA recomb.; Kobas Kor... (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 № 2001/389 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.