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Actim® Partus Test

EUDAMED

Class IVD General (EU MDR)

Ref 31931ETAL

by Actim Oy

Identity

Trade Name
Actim® Partus Test EUDAMED
Device Name
Actim® Partus Test EUDAMED
Model / Reference
31931ETAL EUDAMED

Identifiers

Primary DI / UDI-DI
D-6430030990530TT EUDAMED
Basic UDI-DI
B-6430030990530TT EUDAMED
EMDN Code
W01021699 RAPID TESTS & POINT OF CARE - IMMUNOCHEMISTRY - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Actim® Partus Test by Actim 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
Actim Oy
EUDAMED SRN
FI-MF-000024323

Sources (1)

  • EUDAMED 6c357453-c132-4df8-a0c3-8714ecbc4bc5 61 fields · synced Aug 3, 2026