Dry smallpox diagnostic serum according to TU 21.20.21-065-20401675-2021
Russia·231840·JSC "NPO "Microgen"·Registered February 09, 2022·Class 2b- Device Name (English)
- Dry smallpox diagnostic serum according to TU 21.20.21-065-20401675-2021
- Device Name (Russian)
- Сыворотка диагностическая оспенная сухая по ТУ 21.20.21-065-20401675-2021
- Device Type (English)
- N/A
- Device Type (Russian)
- 231840
- Risk Class
- Class 2b
- OKPD Code
- 21.20.21.110
- Registry Key
- 60572.0
- Registration Number
- ФСР 2009/04191
- Registration Date
- February 09, 2022
- Manufacturer Name (English)
- JSC "NPO "Microgen"
- Manufacturer Name (Russian)
- АО "НПО "Микроген"
- Country (English)
- Russia
- Country (Russian)
- Россия
- Legal Address (English)
- Branch of JSC "NPO "Microgen" in Tomsk "NPO "Virion", Russia, 634040, Tomsk region, Tomsk, Ivanovskogo str., 8
- Legal Address (Russian)
- Филиал АО "НПО "Микроген" в г. Томск "НПО "Вирион", Россия, 634040, Томская область, г. Томск, ул. Ивановского, д. 8
- Manufacturing Address
- 127473, Россия, Москва, 2-й Волконский пер., д. 10
Access comprehensive regulatory information for Dry smallpox diagnostic serum according to TU 21.20.21-065-20401675-2021 in the Russia medical device market through Pure Global AI's free database. This Class 2b medical device is registered under Roszdravnadzor registration number ФСР 2009/04191 and manufactured by JSC "NPO "Microgen". The device was registered on February 09, 2022.
This page provides complete registration details including device type, manufacturer information, country of origin (Russia), 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.