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QuikRead go Plus Instrument

EUDAMED

Class A (EU MDR)

Ref 155376Ref 155377Ref 155375

by Aidian Oy

Identity

Trade Name
QuikRead go Plus Instrument EUDAMED
Device Name
QuikRead go Plus Instrument EUDAMED
Model / Reference
155376 EUDAMED
155377 EUDAMED
155375 EUDAMED

Identifiers

Primary DI / UDI-DI
06438115001690 EUDAMED
06438115001713 EUDAMED
06438115001706 EUDAMED
Basic UDI-DI
6438115QRgoPlusDR EUDAMED
Direct Marketing DI
06438115001690 EUDAMED
06438115001713 EUDAMED
06438115001706 EUDAMED
EMDN Code
W0201020205 TURBIDIMETERS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

QuikRead go Plus Instrument by Aidian Oy — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Aidian Oy
EUDAMED SRN
FI-MF-000023611

Sources (3)

  • EUDAMED 0fcaba73-914a-4674-8809-aa045554be39 61 fields · synced Jul 29, 2026
  • EUDAMED c217e58a-fe2c-4869-99d5-48b483f31caf 61 fields · synced May 18, 2026
  • EUDAMED b857feb8-20fc-479d-b910-b8b48523f9a2 61 fields · synced May 19, 2026