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Venoflex Kokoon

EUDAMED

Class I (EU MDR)

Ref 52200320206012

by Thuasne

Identity

Device Name
Venoflex Kokoon EUDAMED
Model / Reference
52200320206012 EUDAMED

Identifiers

Primary DI / UDI-DI
03111790052586 EUDAMED
Basic UDI-DI
311179FR0001CE5 EUDAMED
Direct Marketing DI
03111790052586 EUDAMED
EMDN Code
M030405 COMPRESSION STOCKINGS 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

Venoflex Kokoon 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 68e9e75b-2e3d-43a1-abb0-ccc417aafce4 61 fields · synced Jun 19, 2026