Jota 9501M.RA.030
by Jota AG
Ref 653204243513030Model Rotary Instruments
Jota 9501M.RA.030 is a device classified as Class IIa in the EU and Class I in the US made by Jota AG, registered in EUDAMED on 26 Jun 2026 (Basic UDI-DI B-EJOT653204243513030) and listed in FDA GUDID since 26 Sep 2023 (UDI-DI EJOT653204243513030), active as of 22 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-EJOT653204243513030 EJOT653204243513030 | Date26 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | NumberEJOT653204243513030 | Date26 Sep 2023 | StatusListed |
Official records
- EUDAMED public site B-EJOT653204243513030
Across registries
- EUDAMED Basic UDI-DI B-EJOT653204243513030 registered 26 Jun 2026 Active
- FDA GUDID UDI-DI EJOT653204243513030 listed 26 Sep 2023 Listed
Timeline
- Listed FDA GUDID EJOT653204243513030
- Registered EUDAMED B-EJOT653204243513030
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Jota
- Generic name
- Dental polishing brush
- Model / reference
- Rotary Instruments EUDAMED653204243513030 EUDAMED9501M.RA.030 GUDID
- Primary DI / UDI-DI
- EJOT653204243513030
- Basic UDI-DI
- B-EJOT653204243513030
- FDA product code
- EJQ
- EMDN code
- Q0199 Odontology devices - other
- GMDN term
- Dental polishing brush
- Device class
- Class IIa EUDAMEDClass I GUDID
- Regulation number
- 872.6010
- 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 |
|---|---|---|
| Model / reference | Rotary Instruments 653204243513030 | 9501M.RA.030 |
| Device class | Class IIa | Class I |
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