Myco-Urea-Chlami-Fluorogen Reagent Kit Diagnosticum for the detection of Mycoplasma hominis, Mycoplasma pneumoniae, Ureaplasma urealyticum and Chlamydia trachomatis antigens in immunofluorescence assay according to TU 9398-114-70423725-2009
Russia·см. приложение·ECOlab JSC·Registered August 07, 2024·Class 2b- Device Name (English)
- Myco-Urea-Chlami-Fluorogen Reagent Kit Diagnosticum for the detection of Mycoplasma hominis, Mycoplasma pneumoniae, Ureaplasma urealyticum and Chlamydia trachomatis antigens in immunofluorescence assay according to TU 9398-114-70423725-2009
- Device Name (Russian)
- Набор реагентов «Мико-Уреа-Хлами-флюороген» Диагностикум для выявления антигенов Mycoplasma hominis, Mycoplasma pneumoniae, Ureaplasma urealyticum и Chlamydia trachomatis в реакции иммунофлюоресценции по ТУ 9398-114-70423725-2009
- Device Type (English)
- N/A
- Device Type (Russian)
- см. приложение
- Risk Class
- Class 2b
- OKPD Code
- 21.20.23.110
- Registry Key
- 80656.0
- Registration Number
- ФСР 2010/09793
- Registration Date
- August 07, 2024
- Manufacturer Name (English)
- ECOlab JSC
- Manufacturer Name (Russian)
- АО "ЭКОлаб"
- Country (English)
- Russia
- Country (Russian)
- Россия
- Legal Address (English)
- ECOlab JSC, 1a, Budennogo Street, Elektrogorsk, Pavlovo-Posadsky, Moscow Region, 142530, Russia
- Legal Address (Russian)
- АО "ЭКОлаб", Россия, 142530, Московская область, г.о. Павлово - Посадский, г. Электрогорск, ул. Буденного, д. 1а
- Manufacturing Address
- 142530, Россия, Московская область, г.о. Павлово-Посадский, г. Электрогорск, ул. Буденного, д. 1
Access comprehensive regulatory information for Myco-Urea-Chlami-Fluorogen Reagent Kit Diagnosticum for the detection of Mycoplasma hominis, Mycoplasma pneumoniae, Ureaplasma urealyticum and Chlamydia trachomatis antigens in immunofluorescence assay according to TU 9398-114-70423725-2009 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 2010/09793 and manufactured by ECOlab JSC. The device was registered on August 07, 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.