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Air Way

EUDAMED

Class IIa (EU MDR)

Ref 5114-ENModel 5114

by VADI Medical Technology Co., Ltd.

Identity

Trade Name
Air Way EUDAMED
Device Name
Air Way EUDAMED
Model / Reference
5114 EUDAMED
5114-EN EUDAMED

Identifiers

Primary DI / UDI-DI
04719894385945 EUDAMED
Basic UDI-DI
B-04719894385945 EUDAMED
EMDN Code
R010199 NASO-OROPHARYNGEAL TUBES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye 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

Air Way 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 (1)

  • EUDAMED 3e8a2407-077e-48ad-85a2-52c800bb73c6 61 fields · synced Jun 18, 2026