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Double Lumen Endobronchial Tube

EUDAMED

Class IIa (EU MDR)

Ref EBT39L(DLT39L)Model Double Lumen Endobronchial Tube

by Ningbo Luke Medical Devices Co., LTD

Identity

Device Name
Double Lumen Endobronchial Tube EUDAMED
Model / Reference
Double Lumen Endobronchial Tube EUDAMED
EBT39L(DLT39L) EUDAMED

Identifiers

Primary DI / UDI-DI
06970240890409 EUDAMED
Basic UDI-DI
697024089EBTPA EUDAMED
Direct Marketing DI
06970240890409 EUDAMED
EMDN Code
R01040202 ENDOBRONCHIAL OROPHARYNGEAL TUBES, LEFT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Hungary EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Double Lumen Endobronchial Tube by Ningbo Luke Medical Devices Co., LTD — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED bd498f73-5513-4ef9-9a63-ab32d071a083 61 fields · synced Aug 2, 2026