A set of reagents for the determination of antibodies to Treponema pallidum in the passive hemagglutination reaction (Syphilis-RPGA test).
- Device Name (English)
- A set of reagents for the determination of antibodies to Treponema pallidum in the passive hemagglutination reaction (Syphilis-RPGA test).
- Device Name (Russian)
- Набор реагентов для определения антител к Treponema pallidum в реакции пассивной гемагглютинации (Сифилис-РПГА-тест).
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- Class 2a
- OKPD Code
- 93 8810
- Registry Key
- o25073
- Registration Number
- ФС 012а2006/5026-06
- Registration Date
- December 28, 2006
- Validity Period
- December 28, 2011
- Manufacturer Name (English)
- CJSC EKOlab
- Manufacturer Name (Russian)
- ЗАО ЭКОлаб
- Country (English)
- Russia
- Country (Russian)
- Россия
- Legal Address (English)
- Moscow. Elektrogorsk, Budennogod str.1
- Legal Address (Russian)
- Моск. обл. г.Электрогорск ул.Буденногод.1
Access comprehensive regulatory information for A set of reagents for the determination of antibodies to Treponema pallidum in the passive hemagglutination reaction (Syphilis-RPGA test). in the Russia medical device market through Pure Global AI's free database. This Class 2a medical device is registered under Roszdravnadzor registration number ФС 012а2006/5026-06 and manufactured by CJSC EKOlab. The device was registered on December 28, 2006.
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.