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Polyflux 17 L

EUDAMED

Class IIb (EU MDR)

Ref Polyflux 17L

by Vantive Health GmbH

Identity

Trade Name
POLYFLUX 17 L EUDAMED
Device Name
Polyflux L EUDAMED
Model / Reference
Polyflux 17L EUDAMED

Identifiers

Primary DI / UDI-DI
07332414200114 EUDAMED
Basic UDI-DI
7332414VA0000142S EUDAMED
EMDN Code
F01060103 DIALYSERS - UFC < 18 ml/h/mmHg, SYNTHETIC MEMBRANES EUDAMED

Classification

Device Class
Class IIb 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

Polyflux 17 L by Vantive Health GmbH — Class IIb — 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
Vantive Health GmbH
EUDAMED SRN
CH-MF-000038981
Authorised Representative
Vantive S.r.l. IT-AR-000041309

Sources (1)

  • EUDAMED a5b139d8-579d-4e65-ab7c-0217626c1857 61 fields · synced Jun 19, 2026