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Endotracheal Tubes for single use

EUDAMED

Class IIa (EU MDR)

Ref ET-Reinforced-Cuff-8.0

by Nanchang Kanghua Health Materials Co., Ltd

Identity

Trade Name
Endotracheal Tubes for single use EUDAMED
Device Name
Endotracheal Tubes for single use EUDAMED
Model / Reference
ET-Reinforced-Cuff-8.0 EUDAMED

Identifiers

Primary DI / UDI-DI
06941730281823 EUDAMED
Basic UDI-DI
B-06941730281823 EUDAMED
EMDN Code
R01030202 ENDOTRACHEAL TUBES, CUFFED, REINFORCED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Category: Reinforced endotracheal tube, single-use

Endotracheal Tubes for single use by Nanchang Kanghua Health Materials 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-000014308
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED 3092f2fd-d120-4951-aa72-24c7e1ba7653 61 fields · synced Sep 18, 2026