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Test Lung

EUDAMED

Class IIa (EU MDR)

Ref G-118000-0-EN1Model G-118000-0

by VADI Medical Technology Co., Ltd.

Identity

Trade Name
Test Lung EUDAMED
Device Name
Test Lung EUDAMED
Model / Reference
G-118000-0 EUDAMED
G-118000-0-EN1 EUDAMED

Identifiers

Primary DI / UDI-DI
04719875340703 EUDAMED
Basic UDI-DI
B-04719875340703 EUDAMED
EMDN Code
R9080 RESPIRATORY AND ANESTHESIA DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Gas-sampling/monitoring respiratory tubing, single-use

Test Lung by VADI Medical Technology Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Gas-sampling/monitoring respiratory tubing, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TW-MF-000022930
Authorised Representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Sources (1)

  • EUDAMED ed87797c-53b5-4fa7-9ca6-3ccbd0be9b0f 61 fields · synced Jun 19, 2026