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Test lung

EUDAMED

Class IIa (EU MDR)

Ref 800-21001-ENModel 800-21001Ref G-118000-0-ACUModel G-118000-0Ref G-118000-0-HM

by VADI Medical Technology Co., Ltd.

Identity

Trade Name
Test lung EUDAMED
Device Name
Test lung EUDAMED
Model / Reference
800-21001 EUDAMED
800-21001-EN EUDAMED
G-118000-0 EUDAMED
G-118000-0-ACU EUDAMED
G-118000-0-HM EUDAMED

Identifiers

Primary DI / UDI-DI
04719875340659 EUDAMED
04719875340741 EUDAMED
04719894383651 EUDAMED
Basic UDI-DI
B-04719875340659 EUDAMED
B-04719875340741 EUDAMED
B-04719894383651 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
Netherlands EUDAMED
Romania 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

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

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 (3)

  • EUDAMED 85ec45af-0a9a-42cc-93ed-058e717094fb 61 fields · synced Jul 31, 2026
  • EUDAMED d1715392-37cb-458b-ab1c-5231f9366f89 61 fields · synced May 17, 2026
  • EUDAMED 6c6b0fe9-a61f-41b7-be1f-b1b1f21b625f 61 fields · synced May 18, 2026