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Disposable Endotracheal Tube

EUDAMED

Class IIa (EU MDR)

Ref /Model Reinforced Type

by Zhejiang Haisheng Medical Device Co., Ltd.

Identity

Device Name
Disposable Endotracheal Tube EUDAMED
Model / Reference
Reinforced Type EUDAMED
/ EUDAMED

Identifiers

Primary DI / UDI-DI
06944375392909 EUDAMED
Basic UDI-DI
B-06944375392909 EUDAMED
EMDN Code
R01030202 ENDOTRACHEAL TUBES, CUFFED, REINFORCED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Reinforced endotracheal tube, single-use

Disposable Endotracheal Tube by Zhejiang Haisheng Medical Device Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Reinforced endotracheal tube, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000026345
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED beed363a-27c6-4ce8-ba09-45d858926596 61 fields · synced Jun 19, 2026