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QuikRead go Instrument

EUDAMED

Class A (EU MDR)

Ref 149915Ref 133893Ref 135867Ref 136196

by Aidian Oy

Identity

Trade Name
QuikRead go Instrument EUDAMED
Device Name
QuikRead go Instrument EUDAMED
Model / Reference
149915 EUDAMED
133893 EUDAMED
135867 EUDAMED
136196 EUDAMED

Identifiers

Primary DI / UDI-DI
06438115001263 EUDAMED
06438115000167 EUDAMED
06438115000181 EUDAMED
06438115000174 EUDAMED
Basic UDI-DI
6438115QRgoInstrumentF8 EUDAMED
Direct Marketing DI
06438115000174 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 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 (4)

  • EUDAMED 30a670b9-e507-4f2a-b264-dc9a0ebc7bf6 61 fields · synced Aug 3, 2026
  • EUDAMED 030b4ffb-2aad-4c83-9ac2-5ab9c4b3d464 61 fields · synced May 18, 2026
  • EUDAMED 1c5eb997-b1c4-4d00-aa27-0a887474325d 61 fields · synced May 18, 2026
  • EUDAMED 2e8c0e72-974d-4759-8d94-540e5a5b9f14 61 fields · synced May 19, 2026