← Back to catalogue

URGOSTART Plus Kompresse

EUDAMED

Class IIb (EU MDR)

Ref 754187

by Laboratoires Urgo

Identity

Trade Name
URGOSTART Plus Kompresse EUDAMED
Device Name
URGOSTART PLUS Pad - URGOSTART PLUS Compresse - URGOSTART PLUS Kompresse EUDAMED
Model / Reference
754187 EUDAMED

Identifiers

Primary DI / UDI-DI
03546890032112 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

URGOSTART Plus Kompresse 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Laboratoires Urgo
EUDAMED SRN
FR-MF-000002559

Sources (1)

  • EUDAMED 57979fba-7d68-4576-a3b8-b9041c85c512 61 fields · synced Jun 18, 2026