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DELFIA Xpress sFlt-1 kit

EUDAMED

Class IVD General (EU MDR)

Ref 6009-001C

by Wallac Oy

Identity

Trade Name
DELFIA Xpress sFlt-1 kit EUDAMED
Device Name
DELFIA Xpress sFlt-1 kit EUDAMED
Model / Reference
6009-001C EUDAMED

Identifiers

Primary DI / UDI-DI
06438147378906 EUDAMED
Basic UDI-DI
B-06438147378906 EUDAMED
EMDN Code
W0102050212 SOLUBLE FMS-LIKE TYROSINE KINASE-1 EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

DELFIA Xpress sFlt-1 kit by Wallac Oy — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

Manufacturer
Wallac Oy
EUDAMED SRN
FI-MF-000022620

Sources (1)

  • EUDAMED bf37a758-9aa4-48ce-92dc-9f25d1152ac2 61 fields · synced Jun 18, 2026