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Polyflux 6h

EUDAMED

Class IIb (EU MDR)

Ref Polyflux 6H

by Vantive Health GmbH

Identity

Trade Name
POLYFLUX 6H EUDAMED
Device Name
Polyflux 6H EUDAMED
Model / Reference
Polyflux 6H EUDAMED

Identifiers

Primary DI / UDI-DI
07332414200015 EUDAMED
Basic UDI-DI
7332414VA00001832 EUDAMED
EMDN Code
F010604 DIALYSERS FOR SPECIAL HAEMODIAFILTRATION AND OTHER THERAPIES 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 6h 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 144c05b0-9761-44ca-b4a3-5edee60af8ea 61 fields · synced Jul 16, 2026