Syntex
by Medisyn Tibbi̇ Ci̇haz Ve Eki̇pmanlar Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ 188 variants
Ref 218.380.01
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number868456405218MB 08684564051658 | Date18 May 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Cystoscopy Packs
- Model / Reference
- 218.380.01
- Primary DI / UDI-DI
- 08684564051658
- Basic UDI-DI
- 868456405218MB
- EMDN Code
- T0202 Surgical procedural kits (excluding surgical instrument kits)
- Device Class
- Class I
- EU market of registration
- Greece
Manufacturer details
- EUDAMED SRN
- TR-MF-000042967
Other devices from Medisyn Tibbi̇ Ci̇haz Ve Eki̇pmanlar Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇
See all devices from Medisyn Tibbi̇ Ci̇haz Ve Eki̇pmanlar Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ →
Properties
Other properties (12)
- 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