Festermed
by Medi̇koki̇m Tibbi̇ Ve Ki̇myevi̇ Malz.san. Ve Ti̇c.a.ş. 4 variants
Ref ALH2001
Active
CE MDR
Valid until
29 May 2030
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number869888147TF03M0339 08698881471808 | Date8 Oct 2026 | StatusActive |
Certificates
- MDR 00068-C Active
Quality management system EU MDR
- Certifier
- KIWA CERMET ITALIA S.P.A. 0476
- Issued
- 30 May 2025
- Expires
- 29 May 2030
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Bilek Gergi Kayışı
- Model / Reference
- ALH2001
- Primary DI / UDI-DI
- 08698881471808
- Basic UDI-DI
- 869888147TF03M0339
- EMDN Code
- M030599 Immobilisation systems and devices - other
- Device Class
- Class I
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000020142
Other devices from Medi̇koki̇m Tibbi̇ Ve Ki̇myevi̇ Malz.san. Ve Ti̇c.a.ş.
See all devices from Medi̇koki̇m Tibbi̇ Ve Ki̇myevi̇ Malz.san. Ve Ti̇c.a.ş. →
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