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Kneo Fem Trial Screw Ø6.5 L20
EUDAMEDClass I (EU MDR)
Ref GKAVF020Model Class Ir Instrument
Identity
- Trade Name
- KNEO FEM TRIAL SCREW Ø6.5 L20 EUDAMED
- Device Name
- Class Ir Instrument EUDAMED
- Model / Reference
- Class Ir Instrument EUDAMEDGKAVF020 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +M483GKAVF0200 EUDAMED
- Basic UDI-DI
- ++M483L0911YN EUDAMED
- Direct Marketing DI
- +M483GKAVF0200 EUDAMED
- EMDN Code
- L091104 ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
The KNEO FEM TRIAL SCREW Ø6.5 L20 is a medical device used for the surgical implantation of femoral prosthetic devices, particularly in knee replacement surgeries. It features a sturdy design with a secure attachment mechanism, making it suitable for various patient scenarios.
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | ++M483L0911YN | Class I | Active |
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Manufacturer
- Manufacturer
- groupe lépine
- EUDAMED SRN
- FR-MF-000001182
Sources (1)
- EUDAMED d7eff5db-612e-4ea5-b0f5-2e1e79b7e5ee 61 fields · synced Jul 25, 2026