← Back to catalogue

Reinforced Endotracheal Tube

EUDAMED

Class IIa (EU MDR)

Ref 91050006Model Cuffled,ID:5.5#

by Guangzhou Orcl Medical Co., Ltd.

Identity

Trade Name
Reinforced Endotracheal Tube EUDAMED
Device Name
Reinforced Endotracheal Tube EUDAMED
Model / Reference
Cuffled,ID:5.5# EUDAMED
91050006 EUDAMED

Identifiers

Primary DI / UDI-DI
06972745360456 EUDAMED
Basic UDI-DI
B-06972745360456 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 Tube 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000039222
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (1)

  • EUDAMED ebf45bbc-36c2-4217-9965-6c7cf4eb1395 61 fields · synced Jun 19, 2026