Mandibular tracker
by ModJaw 4 variants
Ref TIARA2
Mandibular tracker (TIARA2) is a jaw physiology evaluation system (EU MDR Class I; FDA Class I; FDA product code NFS, Device, Jaw Tracking, For Monitoring Jaw Positions) made by Modjaw, registered in EUDAMED on 22 Apr 2024 (Basic UDI-DI 3770022347KITREU5V) and listed in FDA GUDID since 23 Feb 2022 (UDI-DI 03770022347106), 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 | Number3770022347KITREU5V 03770022347106 | Date22 Apr 2024 | StatusActive |
| United States | GUDID listing GUDID | Number03770022347106 | Date23 Feb 2022 | StatusListed |
Official records
- EUDAMED public site 3770022347KITREU5V
- AccessGUDID record 03770022347106
Across registries
- EUDAMED Basic UDI-DI 3770022347KITREU5V registered 22 Apr 2024 Active
- FDA GUDID UDI-DI 03770022347106 listed 23 Feb 2022 Listed
Timeline
- Listed FDA GUDID 03770022347106
- Registered EUDAMED 3770022347KITREU5V
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Rear band
- Generic name
- Jaw physiology evaluation system
- Device name
- Mandibular tracker
- Model / Ref / Catalog
- TIARA2, Rear band
- Primary DI / UDI-DI
- 03770022347106
- Basic UDI-DI
- 3770022347KITREU5V
- Direct marketing DI
- 03770022347106
- FDA product code
- NFS
- EMDN code
- Q0199 Odontology devices - other
- GMDN term
- Jaw physiology evaluation system
- Device class
- Class I
- Regulation number
- 872.2060
- EU registration type
- Standard device
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
Manufacturer details
- EUDAMED SRN
- FR-MF-000009804
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