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QuikRead go CRP

EUDAMED

Class IVD General (EU MDR)

Ref 133891

by Aidian Oy

Identity

Trade Name
QuikRead go CRP EUDAMED
Device Name
QuikRead go CRP EUDAMED
Model / Reference
133891 EUDAMED

Identifiers

Primary DI / UDI-DI
06438115000884 EUDAMED
Basic UDI-DI
B-06438115000884 EUDAMED
EMDN Code
W0102160601 C-REACTIVE PROTEIN - RT & POC 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

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

QuikRead go CRP by Aidian 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
Aidian Oy
EUDAMED SRN
FI-MF-000023611

Sources (1)

  • EUDAMED 1bbd90eb-1aef-4a3c-add9-b94532a6a1b3 61 fields · synced Jun 20, 2026