Sectalon
by Semikal Teknoloji San. ve Tic. A.Ş. 8 variants
Ref AG007, AG009, AG008, AG001, AG107, AG003, AG106
Active
CE MDD
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/MDD | NumberB-08682190075079 | Date30 Apr 2024 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Device Name
- SECTALON Intra-articular GelSECTALON Intra-articular Crosslinked Gel
- Model / Reference
- AG007, AG009, AG008, AG001, AG107, AG003, AG106
- Primary DI / UDI-DI
- 08682190075079, 08684771340439, 08682190075093, 08682190075086, 08684771340422, 08682190075017, 08682190076076, 08684771340415, 08684771340385, 08684771340484, 08684771340361
- Basic UDI-DI
- B-08682190075079, B-08684771340439, B-08682190075093, B-08682190075086, B-08684771340422, B-08682190075017, B-08682190076076, B-08684771340415, B-08684771340385, B-08684771340484, B-08684771340361
- EMDN Code
- P900402 Resorbable filling and reconstruction devices
- Device Class
- Class III
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000024212
Other devices from Semikal Teknoloji San. ve Tic. A.Ş.
Properties
Other properties (9)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No