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Endotracheal Tube

EUDAMED

Class IIa (EU MDR)

Ref SIET0075Model Normal-PVCCuffed,TPUCuffed,Uncuffed,LubriciousCoating,Adaptive-cuff,Suction,Injectable,Supraglottic&SubglotticInjectable,Soft-tip;OralPreformed-PVCCuffed,Uncuffed,LubriciousCoating,Soft-tip;NasalPreformed-PVCCuffed,Uncuffed,LubriciousCoating,Soft-tip

by Henan Tuoren Medical Device Co., Ltd

Identity

Device Name
Endotracheal Tube EUDAMED
Model / Reference
Normal-PVCCuffed,TPUCuffed,Uncuffed,LubriciousCoating,Adaptive-cuff,Suction,Injectable,Supraglottic&SubglotticInjectable,Soft-tip;OralPreformed-PVCCuffed,Uncuffed,LubriciousCoating,Soft-tip;NasalPreformed-PVCCuffed,Uncuffed,LubriciousCoating,Soft-tip EUDAMED
SIET0075 EUDAMED

Identifiers

Primary DI / UDI-DI
16941617110236 EUDAMED
Basic UDI-DI
693811931296J2 EUDAMED
EMDN Code
R01030201 ENDOTRACHEAL TUBES, CUFFED, NOT 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: Basic endotracheal tube, single-use

Endotracheal Tube by Henan Tuoren Medical Device Co., Ltd — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Basic 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-000013924
Authorised Representative
MedNet EC-REP C III GmbH DE-AR-000011196

Sources (1)

  • EUDAMED 93efa3ca-b85f-44e0-a425-8316f6e713fb 61 fields · synced Jun 18, 2026