ELISA reagent kits for the determination of cancer markers in the composition (see attached) Cobas Core AFP EIA - Cobas Core AFP EIA; Cobas Core b-HCG EIA - Cobas Core b-HCG EIA; Кобас Коре СА-125 ИФА - Cobas Core CA-125 EIA; Кобас Коре МРА ИФА - Cobas Core MCA EIA; Kobas Kore REA IFA - C... (see the full description in the card) - Roszdravnadzor Registration МЗ РФ № 2001/387

Access comprehensive regulatory information for ELISA reagent kits for the determination of cancer markers in the composition (see attached) Cobas Core AFP EIA - Cobas Core AFP EIA; Cobas Core b-HCG EIA - Cobas Core b-HCG EIA; Кобас Коре СА-125 ИФА - Cobas Core CA-125 EIA; Кобас Коре МРА ИФА - Cobas Core MCA EIA; Kobas Kore REA IFA - C... (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 № 2001/387 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.