TILT-002 - Tilt Masası Bağlama Kemeri
Ref TILT-002
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 | Number86840557106209L 08684055710620 | Date30 Jun 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- Withdrawn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
- Model / Reference
- TILT-002
- Primary DI / UDI-DI
- 08684055710620
- Basic UDI-DI
- 86840557106209L
- EMDN Code
- V080603 Treatment, diagnosis and monitoring medical beds
- Device Class
- Class I
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000054247
Other devices from Thor Sagli̇k Spor Malzemeleri̇ Ve Rehabi̇li̇taston Si̇stemleri̇ Medi̇kal Yazilim Sanayi̇ Ti̇caret Li̇mi̇ted Si̇rketi̇
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