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endi

by Eyelove Corp Ltd. 249 variants

Ref L Tortoise+2.50

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number471989324EyeLoveZL Basic UDI-DIDate1 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No notified-body 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  • Withdrawn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
Ready-made Reading Spectacles
Model / Reference
L Tortoise+2.50
Primary DI / UDI-DI
04719893242324
Basic UDI-DI
471989324EyeLoveZL
Direct Marketing DI
04719893242324
EMDN Code
Q0210030102 Ready to wear plastic spectacles with organic lenses
Device Class
Class I
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
TW-MF-000033692
Authorised representative
mdi Europa GmbH DE-AR-000006218

Other devices from Eyelove Corp Ltd.

See all devices from Eyelove Corp 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