DURADENT - 0002 - DURABASE LC Işıkla sertleşen kaide plağı/bireysel ölçü kaşığı materyali Light cure base plate
by Erk Dental Med. Tibbi̇. Malz. Tur. San. Ve Ti̇c. Ltd. Şti̇.
Ref 0002
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 | Number869919750002S4 08699197580222 | Date16 Jul 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- Withdrawn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
- DURABASE LC Işıkla sertleşen kaide plağı/bireysel ölçü kaşığı materyali Light cure base plate
- Model / Reference
- 0002
- Primary DI / UDI-DI
- 08699197580222
- Basic UDI-DI
- 869919750002S4
- EMDN Code
- Q010503 Impression material trays, single-use
- Device Class
- Class I
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000038674
Other devices from Erk Dental Med. Tibbi̇. Malz. Tur. San. Ve Ti̇c. Ltd. Şti̇.
See all devices from Erk Dental Med. Tibbi̇. Malz. Tur. San. Ve Ti̇c. Ltd. Şti̇. →
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