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Instrument/analyser IVDs

Australia TGA ARTG Registered Device · Qiagen Pty Ltd · QIAGEN Sciences LLC · Class I · Started February 01, 2017

Good Name: Qiagen Pty Ltd - Instrument/analyser IVDs

Device classification
Risk Class
Class I
Product Type
IVD
ARTG Category
IVD
Registration information
Start Date
February 01, 2017
Effective Date
February 01, 2017
Sponsor
Manufacturer
Country
United States of America
Address
19300 Germantown Road, Germantown, MD, 20874
Intended purpose

Clinical systems and instruments used for assay set up and detection of substances in biological samples.

About this record

Access comprehensive regulatory information for Instrument/analyser IVDs in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Qiagen Pty Ltd, manufactured by QIAGEN Sciences LLC in United States of America. The device registration started on February 01, 2017.

This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.

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