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URGO K2 Latex Free

EUDAMED

Class I (EU MDR)

Ref 552996

by Laboratoires Urgo

Identity

Trade Name
URGO K2 Latex Free EUDAMED
Device Name
URGO K2 Latex Free - URGO KTwo Latex Free EUDAMED
Model / Reference
552996 EUDAMED

Identifiers

Primary DI / UDI-DI
03546890048663 EUDAMED
Basic UDI-DI
354689UM008058 EUDAMED
EMDN Code
M03040199 ELASTIC COMPRESSION BANDAGES - 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

URGO K2 Latex Free by Laboratoires Urgo — 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
Laboratoires Urgo
EUDAMED SRN
FR-MF-000002559

Sources (1)

  • EUDAMED 70de4b94-3bd7-431c-8cc3-a7f0c3132830 61 fields · synced Jul 12, 2026