ORTHOSES, UPPER EXTREMITY
- Risk class
- Class I
- CND nomenclatures code
- Y060699
- Trade name
- Shoulder Activator
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 04711769156414
- Basic UDI
- 471986369CL103DH
- Version date
- December 10, 2024
- Manufacturer last update
- May 26, 2021
- Active status
- No
- Manufacturer name
- OPPO Medical Corp.
- Country
- Taiwan
- Country type
- NON_EU
- Address
- 9F, No. 297, Sec. 4, Chung Hsiao East Rd. Taipei
- peggylin@oppomedical.com
- SRN
- DE-AR-000000085
- Country
- Germany
- Address
- 7 Ernst-Heckel-Straße St. Ingbert
- ear@mt-procons.com
- Telephone
- +49 6894 581020
- Competent authority
- DE/CA70 - Landesamt für Umwelt- und Arbeitsschutz
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Ireland
- Human tissues
- No
- Animal tissues
- No
ORTHOSES, UPPER EXTREMITY - OTHER
Access comprehensive regulatory information for ORTHOSES, UPPER EXTREMITY 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 04711769156414 and manufactured by OPPO Medical Corp. in Taiwan.
This page provides complete registration details including trade name (Shoulder Activator), manufacturer information, authorized representative details, competent authority (DE/CA70 - Landesamt für Umwelt- und Arbeitsschutz), 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.