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Anc06142513
EUDAMEDClass IIa (EU MDR)
Ref ANC06142513Model Trial instruments -Knee
Identity
- Model / Reference
- Trial instruments -Knee EUDAMEDANC06142513 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03700535163481 EUDAMED
- Basic UDI-DI
- 3700535100054Q4 EUDAMED
- Direct Marketing DI
- 03700535163481 EUDAMED
- EMDN Code
- L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
Classification
- Device Class
- Class IIa 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
Anc06142513 by X.nov Medical Technology — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
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 | 3700535100054Q4 | Class IIa | Active |
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Manufacturer
- Manufacturer
- X.nov Medical Technology
- EUDAMED SRN
- CH-MF-000018319
- Authorised Representative
- X.NOV FR-AR-000007682
Sources (1)
- EUDAMED 368c15e3-2908-4d9b-9632-ba05251bb7e2 61 fields · synced Jun 18, 2026