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Metha_55

by Interojo Inc.

Ref T1200

Active European Union

CE MDR

Valid until

14 Aug 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS Belgium NV

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberKR24/00000065 Date2 Sep 2026IssuedStatusActive expires 14 Aug 2029

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • KR24/00000065 Active Supplemented

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    2 Sep 2026
    Expires
    14 Aug 2029
    Reason
    Other

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Soft Contact Lens
Model / Reference
T1200
Primary DI / UDI-DI
8800190045OF060200MGKN, 8800190045OF061200MGL3
Basic UDI-DI
8800190047842PLAHWIOWS, 8800190047842SPOHWIO6W
EMDN Code
Q0210040102 Contact lenses - hydrogel, reusable
Device Class
Class IIa
Special Device Type
Standard soft contact lenses
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
KR-MF-000022687
Authorised representative
Contact Lens Service GmbH DE-AR-000016174

Other devices from Interojo Inc.

See all devices from Interojo Inc. →

Properties

  • 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