Nucleic Acid Extraction-Purification Kit V-VI
- Risk class
- Class A
- CND nomenclatures code
- W0105900101
- Trade name
- Nucleic Acid Extraction-Purification Kit V-VI
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 06955792700765
- Basic UDI
- 69557927S5006E000001QJ
- Version date
- February 21, 2025
- Manufacturer last update
- June 07, 2023
- Active status
- No
- Manufacturer name
- Sansure Biotech Inc.
- Country
- China
- Country type
- NON_EU
- Address
- No.680 Lusong Road, Yuelu District Changsha, Hunan Province
- info@sansure.com.cn
- Name
- Obelis s.a.
- SRN
- BE-AR-000000106
- Country
- Belgium
- Address
- 53 Boulevard Général Wahis Brussels
- regulatory@obelis.net
- Telephone
- +32(2)73 25 954
- Competent authority
- Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
- Applicable legislation
- IVDR (REGULATION (EU) 2017/746 on in vitro diagnostic medical devices)
- Placed on the market
- France
- Human tissues
- No
- Animal tissues
- No
REAGENTS FOR DNA AND/OR RNA EXTRACTION AND PREPARATION: BACTERIA AND/OR VIRUS
Access comprehensive regulatory information for Nucleic Acid Extraction-Purification Kit V-VI in the European Union medical device market through Pure Global AI's free database. This Class A device is registered with EU EUDAMED under Primary DI 06955792700765 and manufactured by Sansure Biotech Inc. in China.
This page provides complete registration details including trade name (Nucleic Acid Extraction-Purification Kit V-VI), manufacturer information, authorized representative details, competent authority (Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.