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Full Rim Titanium Optical Frames

by Wenzhou Sense Optical Co., Ltd.

Ref SOEC103

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 Number697460043FFTQ9 Basic UDI-DI 06974600432094UDI-DIDate26 May 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  • Withdrawn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
Full Rim Titanium Optical Frames
Model / Reference
SOEC103
Primary DI / UDI-DI
06974600432094
Basic UDI-DI
697460043FFTQ9
EMDN Code
Q02100201 Metal spectacle frames without lenses
Device Class
Class I
EU market of registration
Latvia

Manufacturer details

EUDAMED SRN
CN-MF-000009540
Authorised representative
Prolinx GmbH DE-AR-000005129

Other devices from Wenzhou Sense Optical Co., Ltd.

See all devices from Wenzhou Sense 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