Reagent kit for rapid identification of the causative agent of legionellosis "Test strip L. pneumophila 1" according to TU 9398-161-78095326-2012
Russia·243920·State Research Center for Applied Microbiology and Biotechnology of the Federal Service for Surveillance on Consumer Rights Protection and Human Welfare·Registered November 26, 2021·Class 2b- Device Name (English)
- Reagent kit for rapid identification of the causative agent of legionellosis "Test strip L. pneumophila 1" according to TU 9398-161-78095326-2012
- Device Name (Russian)
- Набор реагентов для быстрой идентификации возбудителя легионеллеза "Тест-полоска L. pneumophila 1" по ТУ 9398-161-78095326-2012
- Device Type (English)
- N/A
- Device Type (Russian)
- 243920
- Risk Class
- Class 2b
- OKPD Code
- 21.20.23.110
- Registry Key
- 58314.0
- Registration Number
- РЗН 2013/742
- Registration Date
- November 26, 2021
- 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, Obolensk, ter. "Kvartal A", 10
- Legal Address (Russian)
- ФБУН ГНЦ ПМБ, Россия, 142279, Московская область, г.о. Серпухов, п. Оболенск, тер. "Квартал А", д. 10
- Manufacturing Address
- 142279, Россия, Московская область, городской округ Серпухов, п. Оболенск, территория "Квартал А", д. 24
Access comprehensive regulatory information for Reagent kit for rapid identification of the causative agent of legionellosis "Test strip L. pneumophila 1" according to TU 9398-161-78095326-2012 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 2013/742 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 November 26, 2021.
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.