Buffer negative control material in the Buffer Negative Control Kit cassette for quality control and evaluation of the validity of results on the cobas® 6800 automated system (cobas® Buffer Negative Control Kit) series: G08504
Russia·Unknown·Roche Diagnostics GmbH·Registered June 23, 2020·Class 3- Device Name (English)
- Buffer negative control material in the Buffer Negative Control Kit cassette for quality control and evaluation of the validity of results on the cobas® 6800 automated system (cobas® Buffer Negative Control Kit) series: G08504
- Device Name (Russian)
- Буферный отрицательный контрольный материал в кассете Buffer Negative Control Kit для контроля качества и оценки валидности результатов на системе автоматизированной cobas® 6800 (cobas® Buffer Negative Control Kit) серия: G08504
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- Class 3
- OKPD Code
- 21.20.23.110
- Registry Key
- 44645
- Registration Number
- РЗН 2020/11018
- Registration Date
- June 23, 2020
- Validity Period
- January 01, 2021
- Manufacturer Name (English)
- Roche Diagnostics GmbH
- Manufacturer Name (Russian)
- Рош Диагностикс ГмбХ
- Country (English)
- Germany
- Country (Russian)
- Germany
- Legal Address (English)
- Германия Roche Diagnostics GmbH Sandhofer Strasse 116 68305 Mannheim Germany
- Legal Address (Russian)
- Германия Roche Diagnostics GmbH Sandhofer Strasse 116 68305 Mannheim Germany
- Manufacturing Address
- Roche Molecular Systems Inc. 1080 US Highway 202 South Branchburg New Jersey 08876 USA
Access comprehensive regulatory information for Buffer negative control material in the Buffer Negative Control Kit cassette for quality control and evaluation of the validity of results on the cobas® 6800 automated system (cobas® Buffer Negative Control Kit) series: G08504 in the Russia medical device market through Pure Global AI's free database. This Class 3 medical device is registered under Roszdravnadzor registration number РЗН 2020/11018 and manufactured by Roche Diagnostics GmbH. The device was registered on June 23, 2020.
This page provides complete registration details including device type, manufacturer information, country of origin (Germany), 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.