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Video Laryngoscope for Single Use

by Zhejiang UE Medical Corp. 11 variants

Ref 104000036900Model UED-D Series

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 Number697028348EU000010GY Basic UDI-DI 06937048204555UDI-DIDate4 Sep 2023RegisteredStatusActive

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  • Withdrawn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
Video Laryngoscope for Single Use
Model / Reference
UED-D Series, 104000036900
Primary DI / UDI-DI
06937048204555
Basic UDI-DI
697028348EU000010GY
EMDN Code
Z12021004 Video laryngoscopes
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000003020
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Zhejiang UE Medical Corp.

See all devices from Zhejiang UE Medical Corp. →

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