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Urgo K1

by Laboratoires Urgo France EUDAMED

Ref 605779

EMDN M0304010102

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number354689UM01825H Basic UDI-DIDate20 Feb 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
URGO K1 - URGO KOne
Model / Reference
605779
Primary DI / UDI-DI
03546890050758
Basic UDI-DI
354689UM01825H
EMDN Code
M0304010102 Elastic compression bandages, non-adhesive, medium extensibility (70-140%)
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
FR-MF-000002559

Other devices from Laboratoires Urgo

See all devices from Laboratoires Urgo →

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 03546890050758|354689UM01825H 61 fields · synced 25 Oct 2026