Acutec HeadlessCompression Screw
- Risk class
- Class IIb
- CND nomenclatures code
- P09120603
- Implantable
- Yes
- Reusable
- No
- Measuring function
- No
- Primary DI
- 06943139689545
- Basic UDI
- B-06943139689545
- Version date
- February 19, 2025
- Manufacturer last update
- February 12, 2025
- Active status
- No
- Manufacturer name
- Tianjin Zhengtian Medical Instrument Co., Ltd.
- Country
- China
- Country type
- NON_EU
- Address
- No.318, Jingyi Road, Airport Economic Zone Tianjin
- info@natongroup.com
- Name
- Inion Oy
- SRN
- FI-AR-000046224
- Country
- Finland
- Address
- 2 Lääkärinkatu Tampere
- info@inion.com
- Competent authority
- Finnish Medicines Agency, Supervision and licences, Medical Device Unit
- Applicable legislation
- MDD (Directive 93/42/EEC on Medical Devices)
- Placed on the market
- Portugal
- Market available
- Portugal:None~None, Spain:None~None
- Human tissues
- No
- Animal tissues
- No
CANNULATED SCREWS
Access comprehensive regulatory information for Acutec HeadlessCompression Screw in the European Union medical device market through Pure Global AI's free database. This Class IIb device is registered with EU EUDAMED under Primary DI 06943139689545 and manufactured by Tianjin Zhengtian Medical Instrument Co., Ltd. in China.
This page provides complete registration details including manufacturer information, authorized representative details, competent authority (Finnish Medicines Agency, Supervision and licences, Medical Device Unit), 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.