Dry Culture Media for the Detection of E.coli and Coliform Bacteria "McConkie Broth-GRM" as per TU 9385-079-78095326-2009
- Device Name (English)
- Dry Culture Media for the Detection of E.coli and Coliform Bacteria "McConkie Broth-GRM" as per TU 9385-079-78095326-2009
- Device Name (Russian)
- Питательная среда для обнаружения E.coli и колиформных бактерий сухая "Бульон МакКонки-ГРМ" по ТУ 9385-079-78095326-2009
- Device Type (English)
- N/A
- Device Type (Russian)
- 244830
- Risk Class
- N/A
- OKPD Code
- 20.59.52.150
- Registry Key
- 49613.0
- Registration Number
- ФСР 2009/05627
- Registration Date
- December 31, 2020
- Manufacturer Name (English)
- BU SSC PMB
- Manufacturer Name (Russian)
- БУ ГНЦ ПМБ
- Country (English)
- Russia
- Country (Russian)
- Россия
- Legal Address (English)
- FBI SSC PMB, Russia, 142279, Moscow region, Obolensk, Serpukhov urban district, territory "Kvartal A", 10, bldg. 1
- Legal Address (Russian)
- ФБУН ГНЦ ПМБ, Россия, 142279, Московская область, р.п. Оболенск, городской округ Серпухов, территория "Квартал А", д. 10, стр. 1
- Manufacturing Address
- 142279, Россия, Московская область, р.п. Оболенск, городской округ Серпухов, территория "Квартал А", д. 24
Access comprehensive regulatory information for Dry Culture Media for the Detection of E.coli and Coliform Bacteria "McConkie Broth-GRM" as per TU 9385-079-78095326-2009 in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number ФСР 2009/05627 and manufactured by BU SSC PMB. The device was registered on December 31, 2020.
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.