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Mobiderm Intimate

EUDAMED

Class I (EU MDR)

Ref T57155208000C60

by Thuasne Deutschland GmbH

Identity

Device Name
MOBIDERM INTIMATE EUDAMED
Model / Reference
T57155208000C60 EUDAMED

Identifiers

Primary DI / UDI-DI
04035459373678 EUDAMED
Basic UDI-DI
4035459DE1201B33 EUDAMED
Direct Marketing DI
04035459373678 EUDAMED
EMDN Code
Y090399 CLOTHES, FOOTWEAR AND COVERS FOR PROSTHESES - 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

Mobiderm Intimate by Thuasne Deutschland GmbH — 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

EUDAMED SRN
DE-MF-000006210

Sources (1)

  • EUDAMED 8d245108-cef0-4126-a24d-8ca0d8ab6706 61 fields · synced Jun 19, 2026