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Swivel Flex Tube

EUDAMED

Class IIa (EU MDR)

Ref G-312007-ENModel G-312007

by VADI Medical Technology Co., Ltd.

Identity

Trade Name
Swivel Flex Tube EUDAMED
Device Name
Swivel Flex Tube EUDAMED
Model / Reference
G-312007 EUDAMED
G-312007-EN EUDAMED

Identifiers

Primary DI / UDI-DI
04719875343711 EUDAMED
Basic UDI-DI
B-04719875343711 EUDAMED
EMDN Code
R020202 MOBILE CATHETER MOUNTS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Slovakia 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

Swivel Flex Tube 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 556fad5f-180e-4809-8458-ec54abddbdbe 61 fields · synced Jun 19, 2026