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Ok Night

by MEDLAC S.r.l. Italy EUDAMED

Ref OK NIGHT (DR)Model OK NIGHT

EMDN Q02100499

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805221198LACORTOKU7 Basic UDI-DIDate21 Feb 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Ok Night
Model / Reference
OK NIGHT, OK NIGHT (DR)
Primary DI / UDI-DI
08052211980086
Basic UDI-DI
805221198LACORTOKU7
EMDN Code
Q02100499 Contact lenses - other
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000030386

Other devices from MEDLAC S.r.l.

See all devices from MEDLAC S.r.l. →

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 055d13c6-8b64-4517-a677-294faf9c1ea9 61 fields · synced 24 Oct 2026