← Back to catalogue

Reinforce Endotracheal Tubes with cuff

EUDAMED

Class IIa (EU MDR)

Ref 020080

by Jiangsu Henghong Medical Technology Co., Ltd.

Identity

Trade Name
Reinforce Endotracheal Tubes with cuff EUDAMED
Device Name
Reinforce Endotracheal Tubes with cuff EUDAMED
Model / Reference
020080 EUDAMED

Identifiers

Primary DI / UDI-DI
06975946070421 EUDAMED
Basic UDI-DI
697594607RETWWX 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

Reinforce Endotracheal Tubes with cuff by Jiangsu Henghong Medical Technology 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

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

Manufacturer

EUDAMED SRN
CN-MF-000029455
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED a330d373-84be-48b1-9dc0-bb468ecb318f 61 fields · synced Jun 18, 2026