Reagent kit for the detection of Cytomegalovirus by polymerase chain reaction (CYTOPOL) according to TU 9398-428-17253567-2007
Russia·217820·LLC NPF "Litekh"·Registered February 19, 2024·Class 2b- Device Name (English)
- Reagent kit for the detection of Cytomegalovirus by polymerase chain reaction (CYTOPOL) according to TU 9398-428-17253567-2007
- Device Name (Russian)
- Набор реагентов для обнаружения Цитомегаловируса (Cytomegalovirus) методом полимеразной цепной реакции (ЦИТОПОЛ) по ТУ 9398-428-17253567-2007
- Device Type (English)
- N/A
- Device Type (Russian)
- 217820
- Risk Class
- Class 2b
- OKPD Code
- 21.20.23.110
- Registry Key
- 75861.0
- Registration Number
- ФСР 2007/01269
- Registration Date
- February 19, 2024
- Manufacturer Name (English)
- LLC NPF "Litekh"
- Manufacturer Name (Russian)
- ООО НПФ "Литех"
- Country (English)
- Russia
- Country (Russian)
- Россия
- Legal Address (English)
- NPF Litech LLC, 11 Pererva str., bldg. 29, Moscow, 109651, Russia
- Legal Address (Russian)
- ООО НПФ "Литех", Россия, 109651, г. Москва, ул. Перерва, д. 11, стр. 29
- Manufacturing Address
- 119435, Россия, Москва, ул. Малая Пироговская, д. 1, стр. 3
Access comprehensive regulatory information for Reagent kit for the detection of Cytomegalovirus by polymerase chain reaction (CYTOPOL) according to TU 9398-428-17253567-2007 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 2007/01269 and manufactured by LLC NPF "Litekh". The device was registered on February 19, 2024.
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.