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Dental Light

by Dentis Co., Ltd

Ref D-C-LVSL-V5-202602-ENGModel C500

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 Number88000530C500BX Basic UDI-DI Date29 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  • Withdrawn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
Dental Light
Model / Reference
C500, D-C-LVSL-V5-202602-ENG
Primary DI / UDI-DI
08800266944481, 08800266944603
Basic UDI-DI
88000530C500BX
Direct Marketing DI
08800266944481
08800266944603
EMDN Code
Q0199 Odontology devices - other
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
KR-MF-000012523
Authorised representative
KTR Europe GmbH DE-AR-000005685

Other devices from Dentis Co., Ltd.

See all devices from Dentis 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