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URGOSTART Plus Compresse

EUDAMED

Class IIb (EU MDR)

Ref 754193Ref 754185Ref 754204

by Laboratoires Urgo

Identity

Trade Name
URGOSTART Plus Compresse EUDAMED
Device Name
URGOSTART PLUS Pad - URGOSTART PLUS Compresse - URGOSTART PLUS Kompresse EUDAMED
Model / Reference
754193 EUDAMED
754185 EUDAMED
754204 EUDAMED

Identifiers

Primary DI / UDI-DI
03546890040285 EUDAMED
03546890040216 EUDAMED
03546890029266 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 Compresse 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 (3)

  • EUDAMED f4a65688-7de0-4cc6-875f-6fb49897bb2b 61 fields · synced Aug 3, 2026
  • EUDAMED e629de99-9212-4e6c-806e-7e51915c4b8c 61 fields · synced May 17, 2026
  • EUDAMED a7dcc59f-fc1e-4fbc-b1d0-332abc0d2ecb 61 fields · synced May 18, 2026