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Femoral posterior augment trial , #1 , 4mm
EUDAMEDClass I (EU MDR)
Ref NMRKS072Model TRIALS
Identity
- Trade Name
- Femoral posterior augment trial , #1 , 4mm EUDAMED
- Model / Reference
- TRIALS EUDAMEDNMRKS072 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08682549539153 EUDAMED
- Basic UDI-DI
- 86804870TLHT EUDAMED
- EMDN Code
- L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Türkiye 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
Femoral posterior augment trial , #1 , 4mm by Normmed Medi̇kal San. Ve Ti̇c. A.ş. — Class I — 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 | 86804870TLHT | Class I | Active |
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Manufacturer
- Manufacturer
- Normmed Medi̇kal San. Ve Ti̇c. A.ş.
- EUDAMED SRN
- TR-MF-000015713
Sources (1)
- EUDAMED b055813f-c648-4c82-a617-c886dc1a99f6 61 fields · synced Sep 18, 2026