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Kit Biflex Hôpital

EUDAMED

Class I (EU MDR)

Ref 13055020399999

by Thuasne

Identity

Device Name
Kit Biflex Hôpital EUDAMED
Model / Reference
13055020399999 EUDAMED

Identifiers

Primary DI / UDI-DI
03111791305032 EUDAMED
Basic UDI-DI
311179FR0085AFM EUDAMED
Direct Marketing DI
03111791305032 EUDAMED
EMDN Code
M0304010101 ELASTIC COMPRESSION BANDAGES, NON-ADHESIVE, LOW EXTENSIBILITY (<70%) 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

Kit Biflex Hôpital 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 dd72d55c-2b3d-4897-a50e-4b64e93e15a2 61 fields · synced Jun 18, 2026