T3 Line 6392695
Ref 6392695
T3 Line 6392695 is a device classified as Class IIa in the EU and Class I in the US made by SIRONA Dental Systems GmbH, registered in EUDAMED on 21 Oct 2026 (Basic UDI-DI B-+E27663926950) and listed in FDA GUDID since 10 Sep 2016 (UDI-DI +E27663926950), 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-+E27663926950 +E27663926950 | Date21 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number+E27663926950 | Date10 Sep 2016 | StatusListed |
Official records
- EUDAMED public site B-+E27663926950
Across registries
- EUDAMED Basic UDI-DI B-+E27663926950 registered 21 Oct 2026 Active
- FDA GUDID UDI-DI +E27663926950 listed 10 Sep 2016 Listed
Timeline
- Listed FDA GUDID +E27663926950
- Registered EUDAMED B-+E27663926950
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- T3 Line E 6 EUDAMEDT3 Line GUDID
- Generic name
- Dental surgical power tool motorized handpiece/set, pneumatic
- Model / reference
- 6392695
- Primary DI / UDI-DI
- +E27663926950 EUDAMEDE27663926950 GUDID
- Basic UDI-DI
- B-+E27663926950
- FDA product code
- EFB
- EMDN code
- Z12110180 Instruments for dental treatment units - hardware accessories
- GMDN term
- Dental surgical power tool motorized handpiece/set, pneumatic
- Device class
- Class IIa EUDAMEDClass I GUDID
- Regulation number
- 872.4200
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Primary DI / UDI-DI | +E27663926950 | E27663926950 |
| Device class | Class IIa | Class I |
| Sterilise before use | No | Yes |
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