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QuikRead go iFOBT

EUDAMED

Class IVD General (EU MDR)

Ref 136189

by Aidian Oy

Identity

Trade Name
QuikRead go iFOBT EUDAMED
Device Name
QuikRead go iFOBT EUDAMED
Model / Reference
136189 EUDAMED

Identifiers

Primary DI / UDI-DI
06438115001027 EUDAMED
Basic UDI-DI
B-06438115001027 EUDAMED
EMDN Code
W0102160203 FECAL OCCULT BLOOD - 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 iFOBT 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 4cea2c94-a99d-4379-9079-82e342619f61 61 fields · synced Jun 18, 2026