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Double Lumen Endobronchial Tube

by Ningbo Luke Medical Devices Co., LTD EUDAMED

Active European Union

Ref EBT39R(DRT39R）Model Double Lumen Endobronchial Tube

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697024089EBTPA Basic UDI-DIDate20 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

No EU certificate is linked to this device in EUDAMED.

Specification

EUDAMED

Device Name
Double Lumen Endobronchial Tube
Model / Reference
Double Lumen Endobronchial Tube, EBT39R(DRT39R）
Primary DI / UDI-DI
06970240890461
Basic UDI-DI
697024089EBTPA
Direct Marketing DI
06970240890461
EMDN Code
R01040102 Endobronchial oropharyngeal tubes, right
Device Class
Class IIa
Market of Registration
Hungary

Manufacturer details

EUDAMED SRN
CN-MF-000011732
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Other devices from Ningbo Luke Medical Devices Co., LTD

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Properties

  • Sterile

Other properties (12)

  • 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