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Rose K2 KC Optimum Extra Red

by Multilens AB EUDAMED

Active European Union

Ref N70218Model Corneal trial lenses, Optimum Extra

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number731686cornealTrialOEMTSJZ Basic UDI-DIDate28 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Model / Reference
Corneal trial lenses, Optimum Extra, N70218
Primary DI / UDI-DI
731686N70218RL
Basic UDI-DI
731686cornealTrialOEMTSJZ
EMDN Code
Q02100402 Contact lenses - non hydrogel
Device Class
Class I
Special Device Type
Standard Rigid Gas Permeable (RGP) Contact Lenses
Market of Registration
Sweden

Manufacturer details

EUDAMED SRN
SE-MF-000002792

Other devices from Multilens AB

See all devices from Multilens AB →

Properties

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