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URGOSTART Plus Pad

EUDAMED

Class IIb (EU MDR)

Ref 754167

by Laboratoires Urgo

Identity

Trade Name
URGOSTART Plus Pad EUDAMED
Device Name
URGOSTART PLUS Pad - URGOSTART PLUS Compresse - URGOSTART PLUS Kompresse EUDAMED
Model / Reference
754167 EUDAMED

Identifiers

Primary DI / UDI-DI
03546890040124 EUDAMED
Basic UDI-DI
354689UM01054X EUDAMED
EMDN Code
M040499 DRESSINGS FOR WOUNDS, SORES AND ULCERATIONS - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Italy 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

URGOSTART Plus Pad 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 07a0d49b-a058-46e4-8cfe-ab106251fa86 61 fields · synced Jun 20, 2026