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Auto Ref/Keratometer

by Ningbo Ming Sing Optical R&D Co., Ltd. 8 variants

Ref KR-9300Model KR-9000

Active European Union

CE MDR

Valid until

16 Sep 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS Belgium NV

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberCN24/00005857 Date16 Sep 2024IssuedStatusActive expires 16 Sep 2029

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • CN24/00005857 Active

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    16 Sep 2024
    Expires
    16 Sep 2029

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Auto Ref/Keratometer
Model / Reference
KR-9000, KR-9300
Primary DI / UDI-DI
06971821402042
Basic UDI-DI
69718214002V8
Direct Marketing DI
06971821402042
EMDN Code
Q0299 Ophthalmic devices - other
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000012092
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Ningbo Ming Sing Optical R&D Co., Ltd.

See all devices from Ningbo Ming Sing Optical R&D 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