BESNIES LUPUS CURETTE WINDOWED 2MM
- Risk class
- Class I
- CND nomenclatures code
- L0901
- Trade name
- BESNIES LUPUS CURETTE WINDOWED 2MM
- Implantable
- No
- Reusable
- Yes
- Measuring function
- No
- Primary DI
- 89640040179020
- Basic UDI
- 8964004017CUBF253
- Version date
- July 15, 2024
- Manufacturer last update
- April 11, 2024
- Active status
- No
- Manufacturer name
- METECH INTERNATIONAL
- Country
- Pakistan
- Country type
- NON_EU
- Address
- Muslim Street P.O Taj Pura Mubarik Pura, Sialkot
- metechintl1@gmail.com
- SRN
- HU-AR-000034102
- Country
- Hungary
- Address
- 13. al. 1 Budapest, Auróra utca BUDAPEST
- eudamed.representative@gmail.com
- Telephone
- +36706790786
- Competent authority
- Nemzeti Népegészségügyi és Gyógyszerészeti Központ
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Spain
- 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
ORTHOPAEDIC SURGERY SPOONS AND CURETTES, REUSABLE
Access comprehensive regulatory information for BESNIES LUPUS CURETTE WINDOWED 2MM in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 89640040179020 and manufactured by METECH INTERNATIONAL in Pakistan.
This page provides complete registration details including trade name (BESNIES LUPUS CURETTE WINDOWED 2MM), manufacturer information, authorized representative details, competent authority (Nemzeti Népegészségügyi és Gyógyszerészeti Központ ), 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.