Despada Ds 5484 C1 51-20
by Doğan Opti̇k Sanayi̇ Ve Ti̇caret Li̇mi̇ted Şi̇rketi̇
Ref DESPADA DS 5484 C1 51-20Model DESPADA
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number8680274125870-UB41WX 08680274497342 | Date8 Sep 2026 | StatusActive |
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- Withdrawn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 — CE/MDR Active
Specification
- Device Name
- DESPADA spectacle frame
- Model / Reference
- DESPADA, DESPADA DS 5484 C1 51-20
- Primary DI / UDI-DI
- 08680274497342
- Basic UDI-DI
- 8680274125870-UB41WX
- EMDN Code
- Q02100202 Plastic spectacle frames without lenses
- Device Class
- Class I
- EU market of registration
- Poland
Manufacturer details
- EUDAMED SRN
- TR-MF-000058565
Other devices from Doğan Opti̇k Sanayi̇ Ve Ti̇caret Li̇mi̇ted Şi̇rketi̇
See all devices from Doğan Opti̇k Sanayi̇ Ve Ti̇caret Li̇mi̇ted Şi̇rketi̇ →
Properties
Other properties (13)
- 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