gudid Primary ID: 145218

QuikRead go Instrument (UDI 145218)

Manufactured by Aidian Oy

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The QuikRead go Instrument (Model/Catalog Number: 145218) is a medical device manufactured by Aidian Oy. This product is indexed under FDA Product Code / Category Classification JJQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 145218
Product Code / EMDN: JJQ
Device Name: QuikRead go instrument has been designed to measure quantitative test results from patient samples using QuikRead go reagent kits.
Database Sync Date: 2026-08-09 09:24:54

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of QuikRead go Instrument?

The registered manufacturer of record for QuikRead go Instrument is Aidian Oy.

What is the Primary UDI-DI identifier for QuikRead go Instrument?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 145218.

What classification code is assigned to this device?

This device is registered under product classification code JJQ.

Similar Classification Devices (JJQ)

Other Devices by Aidian Oy

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