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Silistab Epi

EUDAMED

Class I (EU MDR)

Ref 23050320200199Ref 23050320500199

by Thuasne

Identity

Device Name
Silistab Epi EUDAMED
Model / Reference
23050320200199 EUDAMED
23050320500199 EUDAMED

Identifiers

Primary DI / UDI-DI
03111790041498 EUDAMED
03111790041528 EUDAMED
Basic UDI-DI
311179FR0015AEJ EUDAMED
Direct Marketing DI
03111790041498 EUDAMED
03111790041528 EUDAMED
EMDN Code
Y060615 ELBOW 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

Silistab Epi 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 (2)

  • EUDAMED aa8f6be3-f1fc-41df-9fdd-6447521b2074 61 fields · synced Jul 9, 2026
  • EUDAMED 53df36cf-0b3f-4f23-9531-366118a3dab6 61 fields · synced May 17, 2026