Disposable Endotracheal Tube

by Zhejiang Haisheng Medical Device Co., Ltd. 160 variants

Ref /Model Reinforced Type

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-06944375392558 Basic UDI-DI 06944375392558UDI-DI	Date24 Dec 2024Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name: Disposable Endotracheal Tube
Model / Reference: Reinforced Type, /

Primary DI / UDI-DI: 06944375392558
Basic UDI-DI: B-06944375392558
EMDN Code: R01030202 Endotracheal tubes, cuffed, reinforced

Device Class: Class IIa
EU market of registration: Spain

Manufacturer details

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

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Properties

Sterile

Other properties (10)

Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No