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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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QuikRead go Instrument — 2 UDI-DI variants, IVDR (Aidian Oy)

MD Atlas
Aidian Oy

Data from EUDAMED, last updated May 23, 2026

QuikRead go Instrument

6438115QRgoInstrumentF8

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Aidian Oy

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Device characteristics

Near-patient testingProfessional testing

Identity & classification

Basic UDI-DI: 6438115QRgoInstrumentF8
Device name: QuikRead go Instrument
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 25, 2022

Manufacturer & authorised representative

Manufacturer

Name: Aidian Oy
SRN: FI-MF-000023611
Country: Finland
Email: eudamed@aidian.eu
Phone: +358 10 309 3000

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G3BDRM3W70GT0F9V2Y16TG2R

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

13389306438115000167
13586706438115000181