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URGOTUL Lite

EUDAMED

Class IIb (EU MDR)

Ref 603293

by Laboratoires Urgo

Identity

Trade Name
URGOTUL Lite EUDAMED
Device Name
URGOTUL Lite EUDAMED
Model / Reference
603293 EUDAMED

Identifiers

Primary DI / UDI-DI
03546890043194 EUDAMED
Basic UDI-DI
354689UM00655C EUDAMED
EMDN Code
M04040602 POLYURETHANE DRESSINGS, COMBINED WITH OTHER SUBSTANCES EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

URGOTUL Lite by Laboratoires Urgo — Class IIb — 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 bf61dfaf-06a0-40cf-9c33-76ad9ab8ca0b 61 fields · synced Jul 11, 2026