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)
Russia·Unknown·F.Hoffmann-La Roche Ltd./ Roche Diagnostics GmbH·Registered April 11, 2001·N/A- Device Name (English)
- 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)
- Device Name (Russian)
- Наборы ИФА реагентов для определения концентрации половых гормонов в составе (см приложение) Кобас Коре Тестостерон ИФА - Cobas Core Testosterone EIA; Кобас Коре Эстрадиол ИФА - Cobas Core Estradiol EIA; Кобас Коре Прогестерон ИФА - Cobas Core Progesterone EIA; Кобас Коре Стероидный разбавител... (см. в карточке полное описание)
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- N/A
- Registry Key
- o61238
- Registration Number
- МЗ РФ № 2001/381
- Registration Date
- April 11, 2001
- Validity Period
- April 11, 2006
- Manufacturer Name (English)
- F.Hoffmann-La Roche Ltd./ Roche Diagnostics GmbH
- Manufacturer Name (Russian)
- F.Hoffmann-La Roche Ltd./ Roche Diagnostics GmbH
- Country (English)
- Switzerland;Germany
- Country (Russian)
- Швейцария;ФРГ
- Legal Address (English)
- Switzerland, Germany
- Legal Address (Russian)
- Швейцария ФРГ
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.