Reagent kits for DCA 2000 express analyzer (see Appendix on 1 sheet) 1. Kit for the determination of glycosylated hemoglobin (HbA1c): 10 reagent cartridges 11 capillaries 1 calibration card 1 instruction 2. Kit for the determination of microalbumin / creatinine: &... (see the full description in the card)
Russia·Unknown·Bayer Corporation·Registered July 30, 2003·N/A- Device Name (English)
- Reagent kits for DCA 2000 express analyzer (see Appendix on 1 sheet) 1. Kit for the determination of glycosylated hemoglobin (HbA1c): 10 reagent cartridges 11 capillaries 1 calibration card 1 instruction 2. Kit for the determination of microalbumin / creatinine: &... (see the full description in the card)
- Device Name (Russian)
- Наборы реагентов к экспресс-анализатору DCA 2000 (см.Приложение на 1 листе) 1.Набор для определения гликолизированного гемоглобина (HbA1c): 10 реагентных картриджей 11 капилляров 1 калибровочная карточка 1 инструкция 2.Набор для определения микроальбумина/креатинина:&... (см. в карточке полное описание)
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- N/A
- Registry Key
- o64441
- Registration Number
- МЗ РФ № 2003/1117
- Registration Date
- July 30, 2003
- Validity Period
- July 30, 2008
- Manufacturer Name (English)
- Bayer Corporation
- Manufacturer Name (Russian)
- Bayer Corporation
- Country (English)
- USA
- Country (Russian)
- USA
- Legal Address (English)
- United States
- Legal Address (Russian)
- США
Access comprehensive regulatory information for Reagent kits for DCA 2000 express analyzer (see Appendix on 1 sheet) 1. Kit for the determination of glycosylated hemoglobin (HbA1c): 10 reagent cartridges 11 capillaries 1 calibration card 1 instruction 2. Kit for the determination of microalbumin / creatinine: &... (see the full description in the card) in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number МЗ РФ № 2003/1117 and manufactured by Bayer Corporation. The device was registered on July 30, 2003.
This page provides complete registration details including device type, manufacturer information, country of origin (USA), 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.