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Disposable Endotracheal Tube

EUDAMED

Class IIa (EU MDR)

Ref 06944803636469Model Reinforce Cuffed, Reinforce Non-Cuffed, Normal Cuffed, Normal Non-cuffed, Reinforce Suction Lumen, Normal Suction Lumen

by Tianjin Plastics Research Institute Co., Ltd.

Identity

Trade Name
Disposable Endotracheal Tube EUDAMED
Device Name
Disposable Endotracheal Tube EUDAMED
Model / Reference
Reinforce Cuffed, Reinforce Non-Cuffed, Normal Cuffed, Normal Non-cuffed, Reinforce Suction Lumen, Normal Suction Lumen EUDAMED
06944803636469 EUDAMED

Identifiers

Primary DI / UDI-DI
06944803636469 EUDAMED
Basic UDI-DI
6944803600020001G3 EUDAMED
EMDN Code
R01030102 ENDOTRACHEAL TUBES, CUFFLESS, REINFORCED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

Disposable Endotracheal Tube by Tianjin Plastics Research Institute 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-000031209
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 8843e3f6-be92-460a-8cde-8030bef95d2c 61 fields · synced Jun 18, 2026