Rebilda Post 1771
by VOCO GmbH
Ref 1771Model Set
Rebilda Post 1771 is a device classified as Class IIa in the EU and Class I in the US made by VOCO GmbH, registered in EUDAMED on 21 Apr 2026 (Basic UDI-DI B-E22117711) and listed in FDA GUDID since 6 Jun 2019 (UDI-DI E22117711), active as of 22 Oct 2026.
Active
CE MDD
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/MDD EUDAMED | NumberB-E22117711 E22117711 | Date21 Apr 2026 | StatusActive |
| United States | GUDID listing GUDID | NumberE22117711 | Date6 Jun 2019 | StatusListed |
Official records
- EUDAMED public site B-E22117711
Across registries
- EUDAMED Basic UDI-DI B-E22117711 registered 21 Apr 2026 Active
- FDA GUDID UDI-DI E22117711 listed 6 Jun 2019 Listed
Timeline
- Listed FDA GUDID E22117711
- Registered EUDAMED B-E22117711
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Rebilda Post
- Generic name
- Pin/post dental drill bit
- Model / Ref / Catalog
- 1771, Set
- Description
- Endodontic post build-up for support and anchorage of coronal restoration in situations with insufficient tooth substance.
- Primary DI / UDI-DI
- E22117711
- Basic UDI-DI
- B-E22117711
- FDA product code
- EKS, DZA, ELR, EBF, KLE, EHQ
- EMDN code
- Z12110180 Instruments for dental treatment units - hardware accessories
- GMDN term
- Pin/post dental drill bit
- Device class
- Class IIa EUDAMEDClass I GUDID
- Regulation number
- 872.4565, 872.4130, 872.3810, 872.3690, 872.3200, 872.3360
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class I |
| Implantable | Yes | No |
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