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URGOSTART Plus Pad

EUDAMED

Class IIb (EU MDR)

Ref 754200

by Laboratoires Urgo

Identity

Trade Name
URGOSTART Plus Pad EUDAMED
Device Name
URGOSTART PLUS Pad - URGOSTART PLUS Compresse - URGOSTART PLUS Kompresse EUDAMED
Model / Reference
754200 EUDAMED

Identifiers

Primary DI / UDI-DI
03546890040254 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
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

Category: Negative-pressure wound therapy system foam dressing, non-antimicrobial

URGOSTART Plus Pad by Laboratoires Urgo — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Negative-pressure wound therapy system foam dressing, non-antimicrobial.

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 c1ae05d7-9113-4107-a2d6-254e71c21a97 61 fields · synced Jun 18, 2026