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CUBE-i 38

by Medios.Ltd South Korea EUDAMED

Ref CUBE-i 38G145870025 EMDN Q0210040102

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number88061529CUBEI38QH Basic UDI-DIDate20 Feb 2023RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Soft Contact Lens
Model / Reference
CUBE-i 38G145870025
Primary DI / UDI-DI
08809938612970
Basic UDI-DI
88061529CUBEI38QH
EMDN Code
Q0210040102 Contact lenses - hydrogel, reusable
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
KR-MF-000027930
Authorised representative
KTR Europe GmbH DE-AR-000005685

Other devices from Medios.Ltd

See all devices from Medios.Ltd →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
Other properties (12)
  • 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 ff4396d5-07ef-4089-811f-7018a97adb9c 61 fields · synced 24 Oct 2026