Ortholox® UHMWPE Spinal Posterior Fixation Dual Band System (f/5.0mm Rod -Ti. Locking) - 5.0 x 250mm
by Ortolog Medi̇kal Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇
Ref 23-004-5250
Active
CE MDR
Valid until
14 Jun 2031
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number868232005SPBSJW 08682320051232 | Date16 Jun 2026 | StatusActive |
Certificates
- MDR.2292-2026/0030 Active
Technical documentation EU MDR
- Certifier
- UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş. 2292
- Issued
- 15 Jun 2026
- Expires
- 14 Jun 2031
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- UHMWPE Spinal Posterior Fixation Dual Band System - Sterile
- Model / Reference
- 23-004-5250
- Primary DI / UDI-DI
- 08682320051232
- Basic UDI-DI
- 868232005SPBSJW
- EMDN Code
- P09070302 Thoracolumbosacral fixation systems
- Device Class
- Class III
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000027137
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Properties
Other properties (11)
- 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