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Prismaflex ST60 set

EUDAMED

Class IIb (EU MDR)

Ref 107643MDR

by Vantive Health GmbH

Identity

Trade Name
Prismaflex ST60 set EUDAMED
Device Name
Prismaflex M set and Prismaflex ST set EUDAMED
Model / Reference
107643MDR EUDAMED

Identifiers

Primary DI / UDI-DI
07332414201432 EUDAMED
Basic UDI-DI
7332414VA0000262Z EUDAMED
EMDN Code
F01060303 DIALYSERS - UFC > 35 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

Prismaflex ST60 set 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 8865c2e6-7f86-4226-b563-cf2b03d271d9 61 fields · synced Jul 22, 2026