Neodent 108.229
by JJGC Indústria e Comércio de Materiais Dentários S/A.
Part of a family of 35 devices: see the family page
Ref 108.229Model Instrument
Neodent 108.229 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 987800095W4) and listed in FDA GUDID since 7 Aug 2024 (UDI-DI 07899878061052), 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 | Number987800095W4 07899878061052 | Date8 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07899878061052 | Date7 Aug 2024 | StatusListed |
Official records
- EUDAMED public site 987800095W4
- AccessGUDID record 07899878061052
Across registries
- EUDAMED Basic UDI-DI 987800095W4 registered 8 May 2026 Active
- FDA GUDID UDI-DI 07899878061052 listed 7 Aug 2024 Listed
Timeline
- Listed FDA GUDID 07899878061052
- Registered EUDAMED 987800095W4
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Neodent
- Generic name
- Dental implant suprastructure, temporary, preformed, reusable
- Device name
- Reusable Implant Impression Copings
- Model / Ref / Catalog
- 108.229, Instrument
- Primary DI / UDI-DI
- 07899878061052
- Basic UDI-DI
- 987800095W4
- FDA product code
- NDP
- EMDN code
- Q0199 Odontology devices - other
- GMDN term
- Dental implant suprastructure, temporary, preformed, 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
- Height — 1.5 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Implantable | No | Yes |
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