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GKS PRIME FLEX: Trial Tibial Baseplate TOP - Size E

EUDAMED

Class IIa (EU MDR)

Ref S53090

by Permedica S.p.A

Identity

Trade Name
GKS PRIME FLEX: Trial Tibial Baseplate TOP - Size E EUDAMED
Device Name
Trial component EUDAMED
Model / Reference
S53090 EUDAMED

Identifiers

Primary DI / UDI-DI
08050323076529 EUDAMED
Basic UDI-DI
B-08050323076529 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 Tibial Baseplate TOP - Size E 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 (1)

  • EUDAMED 608be66b-357b-4846-a30e-f3d2c0fb8c9d 61 fields · synced Jul 10, 2026