CAD/CAM Software 6820893
Ref 6820893
CAD/CAM Software 6820893 is a device classified as Class I in the EU and Class II in the US made by SIRONA Dental Systems GmbH, registered in EUDAMED on 16 Oct 2026 (Basic UDI-DI B-+E27668208930) and listed in FDA GUDID since 8 May 2024 (UDI-DI +E27668208930), active as of 23 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-+E27668208930 +E27668208930 | Date16 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number+E27668208930 | Date8 May 2024 | StatusListed |
Official records
- EUDAMED public site B-+E27668208930
Across registries
- EUDAMED Basic UDI-DI B-+E27668208930 registered 16 Oct 2026 Active
- FDA GUDID UDI-DI +E27668208930 listed 8 May 2024 Listed
Timeline
- Listed FDA GUDID +E27668208930
- Registered EUDAMED B-+E27668208930
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Cerec Sw V5.3 EUDAMEDCAD/CAM Software GUDID
- Generic name
- CAD/CAM software
- Model / Ref / Catalog
- 6820893
- Primary DI / UDI-DI
- +E27668208930 EUDAMEDE27668208930 GUDID
- Basic UDI-DI
- B-+E27668208930
- FDA product code
- PNP, NHA
- EMDN code
- Z11069092 Various digital bioimaging management instruments - medical device software
- GMDN term
- CAD/CAM software
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 872.3630
- 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 |
|---|---|---|
| Primary DI / UDI-DI | +E27668208930 | E27668208930 |
| Device class | Class I | Class II |
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