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GKS PRIME FLEX: TRIAL FEMUR, Flat Inner, Titanium - Size 5 LEFT

EUDAMED

Class IIa (EU MDR)

Ref S54474Ref S54473

by Permedica S.p.A

Identity

Trade Name
GKS PRIME FLEX: TRIAL FEMUR, Flat Inner, Titanium - Size 5 LEFT EUDAMED
GKS PRIME FLEX: TRIAL FEMUR, Flat Inner, Titanium - Size 5 RIGHT EUDAMED
Device Name
Trial component EUDAMED
Model / Reference
S54474 EUDAMED
S54473 EUDAMED

Identifiers

Primary DI / UDI-DI
08050323151059 EUDAMED
08050323151042 EUDAMED
Basic UDI-DI
B-08050323151059 EUDAMED
B-08050323151042 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: TRIAL FEMUR, Flat Inner, Titanium - Size 5 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

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Manufacturer

Manufacturer
Permedica S.p.A
EUDAMED SRN
IT-MF-000008110

Sources (2)

  • EUDAMED b0bbbff0-b9d3-4664-991f-869c4f53d059 61 fields · synced Jul 21, 2026
  • EUDAMED 906718bc-a975-410e-90d0-a1ea8b124ea3 61 fields · synced May 18, 2026