High-Definition Custom Silicone
- Risk class
- Class I
- CND nomenclatures code
- Y061803
- Trade name
- Finger (premium) 4 digits
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 50633685480222
- Basic UDI
- 50553482ASCTU
- Version date
- November 28, 2024
- Manufacturer last update
- July 20, 2021
- Active status
- No
- Manufacturer name
- Hugh Steeper Limited
- Country
- United Kingdom (ex Northern Ireland)
- Country type
- NON_EU
- Address
- Unit 3, Stourton Link, LS10 1DF Leeds
- tony.coulson@steepergroup.com
- SRN
- NL-AR-000000116
- Country
- Netherlands
- Address
- 60 Westervoortsedijk Arnhem
- lst.aus.euauthrep@ul.com
- Telephone
- +31 70 345 8570
- Competent authority
- Ministerie van Volksgezondheid, Welzijn en Sport
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Netherlands
- Human tissues
- No
- Animal tissues
- No
PARTIAL HAND PROSTHESES (INCLUDING FINGERS PROSTHESES)
Access comprehensive regulatory information for High-Definition Custom Silicone 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 50633685480222 and manufactured by Hugh Steeper Limited in United Kingdom (ex Northern Ireland).
This page provides complete registration details including trade name (Finger (premium) 4 digits), 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.