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Venoflex Kokoon

EUDAMED

Class I (EU MDR)

Ref 52200320204222

by Thuasne

Identity

Device Name
Venoflex Kokoon EUDAMED
Model / Reference
52200320204222 EUDAMED

Identifiers

Primary DI / UDI-DI
03111790052661 EUDAMED
Basic UDI-DI
311179FR0001CE5 EUDAMED
Direct Marketing DI
03111790052661 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

Category: Compression/pressure sock/stocking, single-use

Venoflex Kokoon by Thuasne — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, single-use.

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 4ab71cbe-3458-4a5c-ad8e-865918fe40f1 61 fields · synced Jun 19, 2026