← Back to catalogue
GKS PRIME FLEX: PS Trial FEMUR - Size 4 LEFT
EUDAMEDClass IIa (EU MDR)
Ref S54402
Identity
- Trade Name
- GKS PRIME FLEX: PS Trial FEMUR - Size 4 LEFT EUDAMED
- Device Name
- Trial Component EUDAMED
- Model / Reference
- S54402 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08050323070572 EUDAMED
- Basic UDI-DI
- B-08050323070572 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: PS Trial FEMUR - Size 4 LEFT 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-08050323070572 | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Permedica S.p.A
- EUDAMED SRN
- IT-MF-000008110
Sources (1)
- EUDAMED 74c1c15d-7810-4d27-acf0-3a18cf0b937d 61 fields · synced Jun 19, 2026