gudid Primary ID: 145215

QuikRead go CRP (UDI 145215)

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 CRP (Model/Catalog Number: 145215) is a medical device manufactured by Aidian Oy. This product is indexed under FDA Product Code / Category Classification DCK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 145215
Product Code / EMDN: DCK
Device Name: QuikRead go CRP test is an immunoturbidimetric assay for the in vitro quantitative determination of C-reactive protein (CRP). The test is carried out by means of the QuikRead go instrument.
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 CRP?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 145215.

What classification code is assigned to this device?

This device is registered under product classification code DCK.

Similar Classification Devices (DCK)

Other Devices by Aidian Oy

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