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Genu-Go Silistab

EUDAMED

Class I (EU MDR)

Ref 23430120300599

by Thuasne

Identity

Device Name
Genu-Go Silistab EUDAMED
Model / Reference
23430120300599 EUDAMED

Identifiers

Primary DI / UDI-DI
03111790082583 EUDAMED
Basic UDI-DI
311179FR0016DET EUDAMED
Direct Marketing DI
03111790082583 EUDAMED
EMDN Code
Y061209 KNEE ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Genu-Go Silistab by Thuasne — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Thuasne
EUDAMED SRN
FR-MF-000001201

Sources (1)

  • EUDAMED 2d5836d3-5e31-41ae-a83b-8a1fefd93217 61 fields · synced Jun 18, 2026