Newclip Instruments ANC106
Part of a family of 84 devices: see the family page
Ref ANC106
Newclip Instruments ANC106 is a device classified as Class IIa in the EU and Class I in the US made by Newclip Technics, registered in EUDAMED on 2 Jul 2026 (Basic UDI-DI 3700569600679G) and listed in FDA GUDID since 7 Nov 2024 (UDI-DI 03700569619596), active as of 23 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 | Number3700569600679G 03700569619596 | Date2 Jul 2026 | StatusActive |
| United States | GUDID listing GUDID | Number03700569619596 | Date7 Nov 2024 | StatusListed |
Official records
- EUDAMED public site 3700569600679G
- AccessGUDID record 03700569619596
Across registries
- EUDAMED Basic UDI-DI 3700569600679G registered 2 Jul 2026 Active
- FDA GUDID UDI-DI 03700569619596 listed 7 Nov 2024 Listed
Timeline
- Listed FDA GUDID 03700569619596
- Registered EUDAMED 3700569600679G
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Newclip Instruments
- Generic name
- Fluted surgical drill bit, reusable
- Device name
- Instruments for trauma and orthopaedic surgery
- Model / Ref / Catalog
- ANC106
- Primary DI / UDI-DI
- 03700569619596
- Basic UDI-DI
- 3700569600679G
- FDA product code
- HTW
- EMDN code
- Z12130503 Orthopaedic surgical drills
- GMDN term
- Fluted surgical drill bit, reusable
- Device class
- Class IIa EUDAMEDClass I GUDID
- Regulation number
- 888.4540
- EU registration type
- Standard device
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class I |
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