Femurplatte, proximal, monoaxial winkelstabil, einläufig, rechts, 10 Loch, Titan
Ref S750.536140Model Femurplatte, proximal, monoaxial winkelstabil, einläufig, rechts, 10 Loch, Titan
Active
CE MDR 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 | Number4052024-ws-Platte+TB 04052024082513 | Date14 Oct 2026 | StatusActive |
| European Union | CE/MDR | Number4052024-ws-Platte+TB 04052024082513 | Date14 Oct 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD, CE/MDR Active
Specification
- Device Name
- winkelstabile Platten
- Model / Reference
- S750.536140, Femurplatte, proximal, monoaxial winkelstabil, einläufig, rechts, 10 Loch, Titan
- Primary DI / UDI-DI
- 04052024082513
- Basic UDI-DI
- 4052024-ws-Platte+TB, B-04052024082513
- EMDN Code
- P09120502 Osteosynthesis neutralisation and support plates
- Device Class
- Class IIb
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000005084
Other devices from INTERCUS GmbH
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