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Adraga

by Red Eyewear Ltd 55 variants

Ref ODECEIXEModel PLASTIC FULL RIM

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506026344MSREDRBEVL Basic UDI-DI 05056606113847UDI-DIDate24 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Magnifying Spectacle
Model / Reference
PLASTIC FULL RIM, ODECEIXE
Primary DI / UDI-DI
05056606113847
Basic UDI-DI
506026344MSREDRBEVL
EMDN Code
Q0210030199 Ready to wear spectacles with organic lenses - other
Device Class
Class I
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
HK-MF-000002192
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Red Eyewear Ltd

See all devices from Red Eyewear Ltd →

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