Neodent 125.188
by JJGC Indústria e Comércio de Materiais Dentários S/A.
Part of a family of 70 devices: see the family page
Ref 125.188Model Instrument
Neodent 125.188 is a Class I device made by JJGC Indústria e Comércio de Materiais Dentários S/A., registered in EUDAMED on 8 May 2026 (Basic UDI-DI 987800054VN) and listed in FDA GUDID since 13 Jul 2023 (UDI-DI 07899878058236), 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 | Number987800054VN 07899878058236 | Date8 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07899878058236 | Date13 Jul 2023 | StatusListed |
Official records
- EUDAMED public site 987800054VN
- AccessGUDID record 07899878058236
Across registries
- EUDAMED Basic UDI-DI 987800054VN registered 8 May 2026 Active
- FDA GUDID UDI-DI 07899878058236 listed 13 Jul 2023 Listed
Timeline
- Listed FDA GUDID 07899878058236
- Registered EUDAMED 987800054VN
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Neodent
- Generic name
- Surgical drill guide, reusable
- Device name
- Surgically Invasive Accessories
- Model / Ref / Catalog
- 125.188, Instrument
- Primary DI / UDI-DI
- 07899878058236
- Basic UDI-DI
- 987800054VN
- FDA product code
- NDP
- EMDN code
- L99 Surgical instruments, reusable - other
- GMDN term
- Surgical drill guide, reusable
- 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
- Size
- Length — 8.5 MillimeterLumen/Inner Diameter — 5.2 Millimeter
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