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GKS PRIME FLEX: Tibia TRASER, Trial Baseplate - Size E LEFT

EUDAMED

Class IIa (EU MDR)

Ref S53223

by Permedica S.p.A

Identity

Trade Name
GKS PRIME FLEX: Tibia TRASER, Trial Baseplate - Size E LEFT EUDAMED
Device Name
Trial Component EUDAMED
Model / Reference
S53223 EUDAMED

Identifiers

Primary DI / UDI-DI
08050323124374 EUDAMED
Basic UDI-DI
B-08050323124374 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: Tibia TRASER, Trial Baseplate - Size E 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 (1)

  • EUDAMED 166f2606-c3cc-4aa0-9b81-c2d113b2fbe2 61 fields · synced Aug 2, 2026