Newclip Instruments ANC1087
Part of a family of 60 devices: see the family page
Ref ANC1087
Newclip Instruments ANC1087 is a Class I device made by Newclip Technics, registered in EUDAMED on 2 Jul 2026 (Basic UDI-DI 3700569600418W) and listed in FDA GUDID since 7 Nov 2024 (UDI-DI 03700569631031), active as of 24 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number3700569600418W 03700569631031 | Date2 Jul 2026 | StatusActive |
| United States | GUDID listing GUDID | Number03700569631031 | Date7 Nov 2024 | StatusListed |
Official records
- EUDAMED public site 3700569600418W
- AccessGUDID record 03700569631031
Across registries
- EUDAMED Basic UDI-DI 3700569600418W registered 2 Jul 2026 Active
- FDA GUDID UDI-DI 03700569631031 listed 7 Nov 2024 Listed
Timeline
- Listed FDA GUDID 03700569631031
- Registered EUDAMED 3700569600418W
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Newclip Instruments
- Generic name
- General internal orthopaedic fixation system implantation kit
- Device name
- Instruments for trauma and orthopaedic surgery
- Model / Ref / Catalog
- ANC1087
- Primary DI / UDI-DI
- 03700569631031
- Basic UDI-DI
- 3700569600418W
- FDA product code
- HTZ
- EMDN code
- L0923 Orthopaedics surgical measurers, reusable
- GMDN term
- General internal orthopaedic fixation system implantation kit
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Standard device
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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