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QuikRead go CRP+Hb

EUDAMED

Class IVD General (EU MDR)

Ref 140066Ref 140068

by Aidian Oy

Identity

Trade Name
QuikRead go CRP+Hb EUDAMED
Device Name
QuikRead go CRP+Hb EUDAMED
Model / Reference
140066 EUDAMED
140068 EUDAMED

Identifiers

Primary DI / UDI-DI
06438115000938 EUDAMED
06438115001157 EUDAMED
Basic UDI-DI
B-06438115000938 EUDAMED
B-06438115001157 EUDAMED
EMDN Code
W0102160601,W0103010601 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+Hb 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 (2)

  • EUDAMED 885bbc46-75aa-47fd-a0fd-67c6f3d55f12 61 fields · synced Jul 30, 2026
  • EUDAMED 5fc177c5-73d7-41ac-8832-9a25f9c85864 61 fields · synced May 18, 2026