IonoStar Plus 2545
by VOCO GmbH
Ref 2545
IonoStar Plus 2545 is a device classified as Class IIa in the EU and Class II in the US made by VOCO GmbH, registered in EUDAMED on 30 Mar 2026 (Basic UDI-DI ++E221021200000000074) and listed in FDA GUDID since 13 Sep 2016 (UDI-DI E22125451), active as of 22 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 | Number++E221021200000000074 E22125451 | Date30 Mar 2026 | StatusActive |
| United States | GUDID listing GUDID | NumberE22125451 | Date13 Sep 2016 | StatusListed |
Official records
- EUDAMED public site ++E221021200000000074
Across registries
- EUDAMED Basic UDI-DI ++E221021200000000074 registered 30 Mar 2026 Active
- FDA GUDID UDI-DI E22125451 listed 13 Sep 2016 Listed
Timeline
- Listed FDA GUDID E22125451
- Registered EUDAMED ++E221021200000000074
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- IonoStar Plus
- Generic name
- Glass ionomer dental cement
- Model / Ref / Catalog
- 2545
- Primary DI / UDI-DI
- E22125451
- Basic UDI-DI
- ++E221021200000000074
- FDA product code
- EMA
- EMDN code
- Q01010106 Dental restoration glass ionomers
- GMDN term
- Glass ionomer dental cement
- Device class
- Class IIa EUDAMEDClass II GUDID
- Regulation number
- 872.3275
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class II |
| Implantable | Yes | No |
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