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Optical

by Wenzhou Well Optical Co., Ltd 82 variants

Ref 06978608002662Model OPKEK130304C3

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697860800OPKEK130304C3FA Basic UDI-DI 06978608002662UDI-DIDate21 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

Poland
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

  • Poland

Specification

EUDAMED

Device Name
Optical
Model / Reference
OPKEK130304C3, 06978608002662
Primary DI / UDI-DI
06978608002662
Basic UDI-DI
697860800OPKEK130304C3FA
Direct Marketing DI
06978608002662
EMDN Code
Q02100203 Metal and plastic spectacle frames without lenses
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
CN-MF-000047314
Authorised representative
Humiss International B.V. NL-AR-000001490

Other devices from Wenzhou Well Optical Co., Ltd

See all devices from Wenzhou Well Optical Co., 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