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V3 3v

EUDAMED

Class IIa (EU MDR)

Ref V3 3VR

by Go Medical Industries Pty Ltd

Identity

Trade Name
V3 3V EUDAMED
Device Name
V-set EUDAMED
Model / Reference
V3 3VR EUDAMED

Identifiers

Primary DI / UDI-DI
9350902000099 EUDAMED
Basic UDI-DI
93509020V-SetQ5 EUDAMED
EMDN Code
A070103 INFUSION TUBING ADAPTERS AND CONNECTORS 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

V3 3v by Go Medical Industries Pty. Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
AU-MF-000018687
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED d633dd1e-1813-4727-acec-97f320a25ed8 61 fields · synced Jun 18, 2026