Combined external fixator
- Risk class
- Class I
- CND nomenclatures code
- P09120499
- Trade name
- Combined external fixator
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 06973137576387
- Basic UDI
- 697313757638LH
- Version date
- January 14, 2025
- Manufacturer last update
- June 13, 2024
- Active status
- No
- Manufacturer name
- Beijing Ruibaoli Medical Equipment Co., Ltd.
- Country
- China
- Country type
- NON_EU
- Address
- No.101, Building 1, Courtyard 6, Hengye north seventh street, Tongzhou District Beijing
- xz@bjruibaoli.com
- Name
- MedPath GmbH
- SRN
- DE-AR-000000087
- Country
- Germany
- Address
- 8 Mies-van-der-Rohe-Strasse Munich
- info@medpath.pro
- Telephone
- +49 (0) 89 8130 6837
- Competent authority
- DE/CA304 - Marktüberwachung Medizinprodukte Bayern
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Germany
- Human tissues
- No
- Animal tissues
- No
EXTERNAL BONE FIXATION SYSTEMS - OTHER
Access comprehensive regulatory information for Combined external fixator 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 06973137576387 and manufactured by Beijing Ruibaoli Medical Equipment Co., Ltd. in China.
This page provides complete registration details including trade name (Combined external fixator), manufacturer information, authorized representative details, competent authority (DE/CA304 - Marktüberwachung Medizinprodukte Bayern), 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.