ELISA reagent kits for the determination of hepatitis A markers in the composition (see appendix) Cobas Core anti-HAV EIA; Кобас Коре анти-ВГА IgM ИФА - Cobas Core fnti-HAV IgM EIA.
Russia·Unknown·F.Hoffmann-La Roche Ltd./ Roche Diagnostics GmbH·Registered April 11, 2001·N/A- Device Name (English)
- ELISA reagent kits for the determination of hepatitis A markers in the composition (see appendix) Cobas Core anti-HAV EIA; Кобас Коре анти-ВГА IgM ИФА - Cobas Core fnti-HAV IgM EIA.
- Device Name (Russian)
- Наборы ИФА реагентов для определения маркеров гепатита А в составе (см приложение) Кобас Коре анти-ВГА ИФА - Cobas Core anti-HAV EIA; Кобас Коре анти-ВГА IgM ИФА - Cobas Core fnti-HAV IgM EIA.
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- N/A
- Registry Key
- o61241
- Registration Number
- МЗ РФ № 2001/388
- 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 the determination of hepatitis A markers in the composition (see appendix) Cobas Core anti-HAV EIA; Кобас Коре анти-ВГА IgM ИФА - Cobas Core fnti-HAV IgM EIA. in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number МЗ РФ № 2001/388 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.