A set of reagents for the quantitative determination of uric acid content by the enzymatic method in blood serum and urine (URIC ACID PS DDS)
Russia·Unknown·CJSC Diakon-DS·Registered April 14, 2006·N/A- Device Name (English)
- A set of reagents for the quantitative determination of uric acid content by the enzymatic method in blood serum and urine (URIC ACID PS DDS)
- Device Name (Russian)
- Набор реагентов для количественного определения содержания мочевой кислоты ферментативным методом в сыворотке крови и моче (МОЧЕВАЯ КИСЛОТА ФС ДДС)
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- N/A
- Registry Key
- o28189
- Registration Number
- ФС 012б3040/2825-06
- Registration Date
- April 14, 2006
- Validity Period
- April 14, 2011
- Manufacturer Name (English)
- CJSC Diakon-DS
- Manufacturer Name (Russian)
- ЗАО Диакон-ДС
- Country (English)
- Russia
- Country (Russian)
- Россия
- Legal Address (English)
- Pushchino, Moscow region.
- Legal Address (Russian)
- г.Пущино Московская обл.
Access comprehensive regulatory information for A set of reagents for the quantitative determination of uric acid content by the enzymatic method in blood serum and urine (URIC ACID PS DDS) in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number ФС 012б3040/2825-06 and manufactured by CJSC Diakon-DS. The device was registered on April 14, 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.