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GKS PRIME FLEX RK: Trial Tibia v2 - Size B
EUDAMEDClass IIa (EU MDR)
Ref S47843
Identity
- Trade Name
- GKS PRIME FLEX RK: Trial Tibia v2 - Size B EUDAMED
- Device Name
- Trial Component EUDAMED
- Model / Reference
- S47843 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08050323166206 EUDAMED
- Basic UDI-DI
- B-08050323166206 EUDAMED
- EMDN Code
- V06010102 KNEE PROSTHESES TESTING DEVICES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
GKS PRIME FLEX RK: Trial Tibia v2 - Size B by Permedica S.p.A — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08050323166206 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Permedica S.p.A
- EUDAMED SRN
- IT-MF-000008110
Sources (1)
- EUDAMED b2cebb71-c6d9-41b4-a354-935ed4be20f4 61 fields · synced Jun 19, 2026