Skip to content

Spectacle Lenses

by Shanghai Conant Optics Co., Ltd. 11 variants

Ref Diameter(50-90mm)1.60 ASP FSV UV++ SH-HT

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 Number6974064013231463J5 Basic UDI-DI 06974064011750UDI-DIDate5 Jul 2025RegisteredStatusActive

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  • Withdrawn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
Spectacle Lenses
Model / Reference
Diameter(50-90mm)1.60 ASP FSV UV++ SH-HT
Primary DI / UDI-DI
06974064011750
Basic UDI-DI
6974064013231463J5
EMDN Code
Q0210030101, Q0210030102, Q0210030103, Q0210030199, Q0210030201, Q0210030202, Q0210030203, Q0210030299
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000020231
Authorised representative
Kingsmead Service B.V. NL-AR-000002066

Other devices from Shanghai Conant Optics Co., Ltd.

See all devices from Shanghai Conant Optics 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