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Endotracheal Tube

EUDAMED

Class IIa (EU MDR)

Ref PA030485Model Reinforced with cuff

by Hangzhou Formed Medical Devices Co., Ltd.

Identity

Trade Name
Endotracheal Tube EUDAMED
Device Name
Endotracheal Tube EUDAMED
Model / Reference
Reinforced with cuff EUDAMED
PA030485 EUDAMED

Identifiers

Primary DI / UDI-DI
06923310904322 EUDAMED
Basic UDI-DI
69233109PA03048H 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 Tube by Hangzhou Formed Medical Devices Co., Ltd. — Class IIa — MDR — 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/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000011212
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 02d9c622-0976-457d-b7ae-8014b20ee1dd 61 fields · synced Jun 18, 2026