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Double Lumen Endobronchial Tube

by Ningbo Luke Medical Devices Co., LTD EUDAMED

Active European Union

Ref EBT41R(DRT41R）Model Double Lumen Endobronchial Tube

Regulatory status

as of 26 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  • Withdrawn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

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Double Lumen Endobronchial Tube
Model / Reference
Double Lumen Endobronchial Tube, EBT41R(DRT41R）
Primary DI / UDI-DI
06970240890478
Basic UDI-DI
697024089EBTPA
Direct Marketing DI
06970240890478
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

See all devices from Ningbo Luke Medical Devices Co., LTD →

Properties

Show 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