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Actim® CRP

EUDAMED

Class IVD General (EU MDR)

Ref 31034BURef 31031ETACRef 31032ETPL

by Actim Oy

Identity

Trade Name
Actim® CRP EUDAMED
Device Name
Actim® CRP EUDAMED
Model / Reference
31034BU EUDAMED
31031ETAC EUDAMED
31032ETPL EUDAMED

Identifiers

Primary DI / UDI-DI
D-6430030990752UF EUDAMED
D-6430030990127TJ EUDAMED
D-6430030990776UV EUDAMED
Basic UDI-DI
B-6430030990752UF EUDAMED
B-6430030990127TJ EUDAMED
B-6430030990776UV EUDAMED
EMDN Code
W0102160601 C-REACTIVE PROTEIN - RT & POC EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Finland EUDAMED
Poland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMEDEUDAMED

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® CRP 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 (3)

  • EUDAMED 879b9b43-5c36-4290-9038-5fdaedb8f1bd 61 fields · synced Jul 22, 2026
  • EUDAMED 7b91fa3e-d4ae-472b-9dd8-2cb770ddb989 61 fields · synced May 16, 2026
  • EUDAMED 373b7765-ca30-4b5b-87a8-c3900222ed45 61 fields · synced May 18, 2026