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Mobiderm

EUDAMED

Class I (EU MDR)

Ref 37300220400233

by Thuasne

Identity

Device Name
MOBIDERM EUDAMED
Model / Reference
37300220400233 EUDAMED

Identifiers

Primary DI / UDI-DI
03111790242758 EUDAMED
Basic UDI-DI
311179FR0004AEA EUDAMED
Direct Marketing DI
03111790242758 EUDAMED
EMDN Code
M030499 ELASTIC BANDAGES, SUPPORT AND COMPRESSION - OTHER 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, reusable

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

Similar devices

Also classified as Compression/pressure sock/stocking, reusable.

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 d7c92edd-e90e-45aa-9dc4-57aa332dcdcf 61 fields · synced Jun 18, 2026