Ls 221 Göbek Fitiği Mi̇de Korsesi̇ ( Xl )
by Medoksa Medi̇kal Dokuma San. Ve Ti̇c. Ltd. Şti̇.
Ref LS 221
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 | Number869868375LYN0015P | Date8 Jun 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- Withdrawn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
- Trade Name
- Ls 221 Göbek Fitiği Mi̇de Korsesi̇ ( Xl )Ls 221 Göbek Fitiği Mi̇de Korsesi̇ ( L )Ls 221 Göbek Fitiği Mi̇de Korsesi̇ ( M )Ls 221 Göbek Fitiği Mi̇de Korsesi̇ ( S )
- Device Name
- Ortopedi̇k Medi̇kal Ürünler
- Model / Reference
- LS 221
- Primary DI / UDI-DI
- 08698683755236, 08698683755229, 08698683755212, 08698683755205
- Basic UDI-DI
- 869868375LYN0015P
- EMDN Code
- Y060406 Abdominal hernia supports
- Device Class
- Class I
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000038946
Other devices from Medoksa Medi̇kal Dokuma San. Ve Ti̇c. Ltd. Şti̇.
See all devices from Medoksa Medi̇kal Dokuma San. Ve Ti̇c. Ltd. Şti̇. →
Properties
Other properties (12)
- Sterile: No
- Implantable: 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