QuickmatFLEX sectional matrices
Part of a family of 101 devices: see the family page
Ref 6797
QuickmatFLEX sectional matrices (6797) is a Class I device made by Polydentia SA, registered in EUDAMED on 9 Nov 2021 (Basic UDI-DI ++E299METALMATRICESM6) and listed in FDA GUDID since 6 Jul 2022 (UDI-DI +E29967970), active as of 22 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number+E29967970 | Date6 Jul 2022 | StatusListed |
| European Union | CE/MDR EUDAMED | Number++E299METALMATRICESM6 +E29967970 | Date9 Nov 2021 | StatusActive |
Official records
- EUDAMED public site ++E299METALMATRICESM6
Across registries
- EUDAMED Basic UDI-DI ++E299METALMATRICESM6 registered 9 Nov 2021 Active
- FDA GUDID UDI-DI +E29967970 listed 6 Jul 2022 Listed
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Timeline
- Registered EUDAMED ++E299METALMATRICESM6
- Listed FDA GUDID +E29967970
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Dental matrix band, single-use
- Device name
- Metal Matrices
- Model / reference
- 6797
- Primary DI / UDI-DI
- +E29967970 EUDAMEDE29967970 GUDID
- Basic UDI-DI
- ++E299METALMATRICESM6
- FDA product code
- DZN
- EMDN code
- Q01010401 Paper and gutta-percha tips, matrices and wedges for dentistry
- GMDN term
- Dental matrix band, single-use
- Device class
- Class I
- Regulation number
- 872.4565
- EU registration type
- Standard device
- EU market of registration
- Liechtenstein
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Primary DI / UDI-DI | +E29967970 | E29967970 |
Manufacturer details
- EUDAMED SRN
- CH-MF-000008779
- Authorised representative
- IDD International Dental Distributors AG LI-AR-000008367
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