Celtra® Ceram
by Dentsply International 73 variants
Ref 615156Model Celtra Ceram Opaceous Dentin - OD6, 15G
Celtra® Ceram (615156) is a device classified as Class IIa in the EU and Class II in the US made by Dentsply International, registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-D0016151561) and listed in FDA GUDID since 3 Mar 2017 (UDI-DI D0016151561), active as of 7 Nov 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-D0016151561 D0016151561 | Date29 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | NumberD0016151561 | Date3 Mar 2017 | StatusListed |
Official records
- EUDAMED public site B-D0016151561
Across registries
- EUDAMED Basic UDI-DI B-D0016151561 registered 29 Oct 2026 Active
- FDA GUDID UDI-DI D0016151561 listed 3 Mar 2017 Listed
Timeline
- Listed FDA GUDID D0016151561
- Registered EUDAMED B-D0016151561
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Celtra® Ceram EUDAMEDCeltra® GUDID
- Generic name
- Dental appliance fabrication material, ceramic
- Model / Ref / Catalog
- Celtra Ceram Opaceous Dentin - OD6, 15G, 615156, Ceram
- Primary DI / UDI-DI
- D0016151561
- Basic UDI-DI
- B-D0016151561
- FDA product code
- EIH
- EMDN code
- Q010299 Prosthetic dentistry devices - other
- GMDN term
- Dental appliance fabrication material, ceramic
- Device class
- Class IIa EUDAMEDClass II GUDID
- Regulation number
- 872.6660
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Size
- Weight — 15 Gram
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | Celtra Ceram Opaceous Dentin - OD6, 15G 615156 | Ceram |
| Device class | Class IIa | Class II |
| Implantable | Yes | No |
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