Dry culture medium for the isolation of Pseudomonas aeruginosa (CPC agar) according to TU 20.59.52-325-78095326-2020
Russia·217030·State Research Center for Applied Microbiology and Biotechnology of the Federal Service for Surveillance on Consumer Rights Protection and Human Welfare·Registered January 26, 2022·Class 2b- Device Name (English)
- Dry culture medium for the isolation of Pseudomonas aeruginosa (CPC agar) according to TU 20.59.52-325-78095326-2020
- Device Name (Russian)
- Питательная среда для выделения синегнойной палочки сухая (ЦПХ агар) по ТУ 20.59.52-325-78095326-2020
- Device Type (English)
- N/A
- Device Type (Russian)
- 217030
- Risk Class
- Class 2b
- OKPD Code
- 20.59.52.150
- Registry Key
- 55228.0
- Registration Number
- РЗН 2022/16428
- Registration Date
- January 26, 2022
- Manufacturer Name (English)
- State Research Center for Applied Microbiology and Biotechnology of the Federal Service for Surveillance on Consumer Rights Protection and Human Welfare
- Manufacturer Name (Russian)
- БУ "Государственный научный центр прикладной микробиологии и биотехнологии" Федеральной службы по надзору в сфере защиты прав потребителей и благополучия человека
- Country (English)
- Russia
- Country (Russian)
- Россия
- Legal Address (English)
- FBI SSC PMB, Russia, 142279, Moscow Region, Serpukhov Urban District, Obolensk, Kvartal A Territory, 10, bldg. 1
- Legal Address (Russian)
- ФБУН ГНЦ ПМБ, Россия, 142279, Московская область, городской округ Серпухов, п. Оболенск, территория "Квартал А", д. 10, стр. 1
- Manufacturing Address
- 142279, Россия, Московская область, городской округ Серпухов, п. Оболенск, территория "Квартал А", д. 24
Access comprehensive regulatory information for Dry culture medium for the isolation of Pseudomonas aeruginosa (CPC agar) according to TU 20.59.52-325-78095326-2020 in the Russia medical device market through Pure Global AI's free database. This Class 2b medical device is registered under Roszdravnadzor registration number РЗН 2022/16428 and manufactured by State Research Center for Applied Microbiology and Biotechnology of the Federal Service for Surveillance on Consumer Rights Protection and Human Welfare. The device was registered on January 26, 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.