Sefill
by Semikal Teknoloji San. ve Tic. A.Ş. 3 variants
Ref AG007, AG107, AG009, AG106, AG008, AG003, AG004
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-08684771340583 | Date12 Dec 2025 | 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- Withdrawn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
- SEFILL Intra-articular Gel
- Model / Reference
- AG007, AG107, AG009, AG106, AG008, AG003, AG004
- Primary DI / UDI-DI
- 08684771340583, 08684771340668, 08684771340606, 08684771340651, 08684771340590, 08684771340552, 08682190075543
- Basic UDI-DI
- B-08684771340583, B-08684771340668, B-08684771340606, B-08684771340651, B-08684771340590, B-08684771340552, B-08682190075543
- 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