C-Plast 672722
by Candulor AG
Ref 672722
C-Plast 672722 is a dental base plate (EU MDR Class I; FDA Class I; FDA product code EBH, Material, Impression Tray, Resin) made by Candulor AG, registered in EUDAMED on 9 Oct 2026 (Basic UDI-DI 763081341XTRAY0018Z) and listed in FDA GUDID since 14 Nov 2022 (UDI-DI 07630813440033), active as of 25 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 | Number763081341XTRAY0018Z 07630813440033 | Date9 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07630813440033 | Date14 Nov 2022 | StatusListed |
Official records
- EUDAMED public site 763081341XTRAY0018Z
- AccessGUDID record 07630813440033
Across registries
- EUDAMED Basic UDI-DI 763081341XTRAY0018Z registered 9 Oct 2026 Active
- FDA GUDID UDI-DI 07630813440033 listed 14 Nov 2022 Listed
Timeline
- Listed FDA GUDID 07630813440033
- Registered EUDAMED 763081341XTRAY0018Z
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- C-Plast Polymer 500g F34 EUDAMEDC-Plast GUDID
- Generic name
- Dental base plate
- Model / Ref / Catalog
- 672722
- Primary DI / UDI-DI
- 07630813440033
- Basic UDI-DI
- 763081341XTRAY0018Z
- FDA product code
- EBH
- EMDN code
- Q010699 Materials for the preparation of custom-made dental devices - other
- GMDN term
- Dental base plate
- Device class
- Class I
- Regulation number
- 872.3670
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
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