Palodent® V3 Sectional Matrix System Designed by Triodent® 659720V
Ref 659720V
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number++D002MATRIXSYSTEMSPX D002659720V1 | Date16 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | NumberD002659720V1 | Date2 Apr 2019 | StatusListed |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Palodent® V3 Sectional Matrix System Designed by Triodent®
- Generic Name
- Dental matrix band, single-use
- Device Name
- Matrix Systems
- Model / Ref / Catalog
- 659720V
- Primary DI / UDI-DI
- D002659720V1
- Basic UDI-DI
- ++D002MATRIXSYSTEMSPX
- FDA Product Code
- DZN
- EMDN Code
- Q01010199 Dental restoration devices - other
- GMDN Term
- Dental matrix band, single-use
- Device Class
- Class I
- Regulation Number
- 872.4565
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
Other devices from Dentsply International
Properties
Other properties (19)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Manufacturing Date: No