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HI-FLO IV Extension Set

EUDAMED

Class I (EU MDR)

Ref GSS009B02S

by GVS S.p.A.

Identity

Trade Name
HI-FLO IV Extension Set EUDAMED
Device Name
Infusion Devices Class Is EUDAMED
Model / Reference
GSS009B02S EUDAMED

Identifiers

Primary DI / UDI-DI
08053879800365 EUDAMED
Basic UDI-DI
805387980SETINF1S000000CS EUDAMED
EMDN Code
A03020101 LOW PRESSURE EXTENSION LINES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

HI-FLO IV Extension Set by GVS S.p.A. — Class I — 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

Manufacturer
GVS S.p.A.
EUDAMED SRN
IT-MF-000028147

Sources (1)

  • EUDAMED dea07801-809c-4808-9b76-410d9c1ee238 61 fields · synced Jul 22, 2026