Neoss Implant System 51171
by Neoss AB
Part of a family of 10 devices: see the family page
Ref 51171
Neoss Implant System 51171 is a Class I device made by Neoss AB, registered in EUDAMED on 4 Mar 2026 (Basic UDI-DI 506044033N0025MZ) and listed in FDA GUDID since 8 Oct 2015 (UDI-DI 05060440332807), active as of 12 Nov 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 | Number506044033N0025MZ 05060440332807 | Date4 Mar 2026 | StatusActive |
| United States | GUDID listing GUDID | Number05060440332807 | Date8 Oct 2015 | StatusListed |
Official records
- EUDAMED public site 506044033N0025MZ
- AccessGUDID record 05060440332807
Across registries
- EUDAMED Basic UDI-DI 506044033N0025MZ registered 4 Mar 2026 Active
- FDA GUDID UDI-DI 05060440332807 listed 8 Oct 2015 Listed
Timeline
- Listed FDA GUDID 05060440332807
- Registered EUDAMED 506044033N0025MZ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Neoss® Guide - Countersink Conduit Ø5.0 EUDAMEDNeoss Implant System GUDID
- Generic name
- Fixture/appliance dental drill bit, single-use
- Device name
- Guide Accessories
- Model / Ref / Catalog
- 51171
- Primary DI / UDI-DI
- 05060440332807
- Basic UDI-DI
- 506044033N0025MZ
- Direct marketing DI
- 05060440332807
- FDA product code
- NDP
- EMDN code
- P01020180 Dental implants - accessories
- GMDN term
- Fixture/appliance dental drill bit, single-use
- Device class
- Class I
- Regulation number
- 872.3980
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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