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Integrity

by Urathon Europe Limited United Kingdom EUDAMED

Ref 90685 EMDN Y120699

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number03906906855N Basic UDI-DIDate21 Mar 2024RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
Aries Hybrid 2-in-1 Rollator Medium
Model / Reference
90685
Primary DI / UDI-DI
90685
Basic UDI-DI
03906906855N
Direct Marketing DI
90685
EMDN Code
Y120699 Walking devices, two-handed operation - other
Device Class
Class I

Manufacturer details

EUDAMED SRN
UK-MF-000039685
Authorised representative
Ives MD EU Rep Ltd XI-AR-000038402

Other devices from Urathon Europe Limited

See all devices from Urathon Europe Limited →

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 f7253613-3129-481b-ac60-09d4415dd891 61 fields · synced 23 Oct 2026