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URGOSTART Contact

EUDAMED

Class IIb (EU MDR)

Ref 754149

by Laboratoires Urgo

Identity

Trade Name
URGOSTART Contact EUDAMED
Device Name
URGOSTART Contact / URGOSTART Interface / URGOSTART Tül EUDAMED
Model / Reference
754149 EUDAMED

Identifiers

Primary DI / UDI-DI
03546890042142 EUDAMED
Basic UDI-DI
354689UM00745D EUDAMED
EMDN Code
M040499 DRESSINGS FOR WOUNDS, SORES AND ULCERATIONS - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Northern Ireland 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 Contact 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 f7b96eca-f3d3-4f0f-8bc9-04378ab8cd06 61 fields · synced Jun 19, 2026