Real-Time PCR System
- Risk class
- Class A
- CND nomenclatures code
- W02050116
- Trade name
- Real-Time PCR System
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 06972168355015
- Basic UDI
- 6972168353201AA
- Version date
- March 03, 2025
- Manufacturer last update
- September 05, 2022
- Active status
- No
- Manufacturer name
- Maccura Medical Instrument Co., Ltd.
- Country
- China
- Country type
- NON_EU
- Address
- Building 4, 8#, 2nd Anhe Roda, Hi-tech Zone, 611731, Chengdu Chengdu
- maccura@maccura.com
- SRN
- NL-AR-000001490
- Country
- Netherlands
- Address
- 701 Joop Geesinkweg Amsterdam-Duivendrech
- ce-tech@humiss.com
- Telephone
- +31 (0)20 369 8116
- Competent authority
- Ministerie van Volksgezondheid, Welzijn en Sport
- Applicable legislation
- IVDR (REGULATION (EU) 2017/746 on in vitro diagnostic medical devices)
- Placed on the market
- Türkiye
- Market available
- Austria:None~None, Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia:None~None, Denmark:None~None, Estonia:None~None, Finland:None~None, France:None~None, Germany:None~None, Greece:None~None, Hungary:None~None, Iceland:None~None, Ireland:None~None, Italy:None~None, Latvia:None~None, Liechtenstein:None~None, Lithuania:None~None, Luxembourg:None~None, Malta:None~None, Netherlands:None~None, Norway:None~None, Poland:None~None, Portugal:None~None, Romania:None~None, Slovakia:None~None, Slovenia:None~None, Spain:None~None, Sweden:None~None, Türkiye:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
NUCLEIC ACID TESTING INTEGRETED EXTRATION /AMPLIFICATION /DETECTION SYSTEMS
Access comprehensive regulatory information for Real-Time PCR System 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 06972168355015 and manufactured by Maccura Medical Instrument Co., Ltd. in China.
This page provides complete registration details including trade name (Real-Time PCR System), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), 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.