Automatic Hematology Analyzer
- Risk class
- IVD General
- CND nomenclatures code
- W0202010101
- Trade name
- Automatic Hematology Analyzer
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 06972168355671
- Basic UDI
- B-06972168355671
- Version date
- September 14, 2024
- 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
- DE-AR-000000001
- Country
- Germany
- Address
- 80 Eiffestraße Hamburg
- shholding@hotmail.com
- Telephone
- +49 40 2513175
- Competent authority
- Ministerie van Volksgezondheid, Welzijn en Sport
- Applicable legislation
- IVDD (Directive 98/79/EC on in vitro Diagnostic Medical Devices)
- Placed on the market
- Slovenia
- Market available
- 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, Austria:None~None, Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia:None~None, Denmark:None~None, Estonia:None~None
- Human tissues
- No
- Animal tissues
- No
AUTOMATED WHOLE BLOOD HEMATOLOGY ANALYSERS - LOW ROUTINE (Throughput <= 100 samples/hr)
Access comprehensive regulatory information for Automatic Hematology Analyzer in the European Union medical device market through Pure Global AI's free database. This IVD General device is registered with EU EUDAMED under Primary DI 06972168355671 and manufactured by Maccura Medical Instrument Co., Ltd. in China.
This page provides complete registration details including trade name (Automatic Hematology Analyzer), 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.