gudid Primary ID: 1

aLF Reader (UDI 1)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The aLF Reader (Model/Catalog Number: 1) is a medical device manufactured by QIAGEN GmbH. This product is indexed under FDA Product Code / Category Classification JJQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1
Product Code / EMDN: JJQ
Device Name: photometric reader for scanning and interpretation of immunochromatographic assays
Database Sync Date: 2026-08-09 09:26:12

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 aLF Reader?

The registered manufacturer of record for aLF Reader is QIAGEN GmbH.

What is the Primary UDI-DI identifier for aLF Reader?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.

What classification code is assigned to this device?

This device is registered under product classification code JJQ.

Similar Classification Devices (JJQ)

Other Devices by QIAGEN GmbH

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