Reagent kit Enzyme immunoassay system for the detection of IgM antibodies to rubella virus (ELISA-Rubella-IgM).
- Device Name (English)
- Reagent kit Enzyme immunoassay system for the detection of IgM antibodies to rubella virus (ELISA-Rubella-IgM).
- Device Name (Russian)
- Набор реагентов Тест-система иммуноферментная для выявления антител класса IgM к вирусу краснухи (ИФА-Краснуха-IgM).
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- Class 3
- OKPD Code
- 93 8840
- Registry Key
- o25777
- Registration Number
- ФС 01032006/5591-06
- Registration Date
- December 29, 2006
- Validity Period
- December 29, 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 Reagent kit Enzyme immunoassay system for the detection of IgM antibodies to rubella virus (ELISA-Rubella-IgM). in the Russia medical device market through Pure Global AI's free database. This Class 3 medical device is registered under Roszdravnadzor registration number ФС 01032006/5591-06 and manufactured by CJSC EKOlab. The device was registered on December 29, 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.