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Reinforced Endotracheal Tubes

EUDAMED

Class IIa (EU MDR)

Ref 91050001Model Cuffled, ID:3.0#

by Guangzhou Orcl Medical Co., Ltd.

Identity

Trade Name
REINFORCED ENDOTRACHEAL TUBES EUDAMED
Device Name
Reinforced Endotracheal Tube EUDAMED
Model / Reference
Cuffled, ID:3.0# EUDAMED
91050001 EUDAMED

Identifiers

Primary DI / UDI-DI
06972745360401 EUDAMED
Basic UDI-DI
B-06972745360401 EUDAMED
EMDN Code
R01030202 ENDOTRACHEAL TUBES, CUFFED, REINFORCED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Finland 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

Reinforced Endotracheal Tubes by Guangzhou Orcl Medical 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-000039222
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (1)

  • EUDAMED e5a05649-ba50-4b85-8e5d-307f04293924 61 fields · synced Jun 18, 2026