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Specimen receptacle IVDs

Access comprehensive regulatory information for Specimen receptacle 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 NeuMoDx Molecular Inc in United States of America. The device registration started on August 18, 2020.

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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TGA ARTG Official Data
Class I
Class I
Specimen receptacle IVDs
Australia TGA ARTG Registered Device
Good Name: Qiagen Pty Ltd - Specimen receptacle IVDs
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Intended Purpose

IVDs that are vessels with or without additives that are intended to be used for the collection, containment, preservation and/or transport of all clinical specimens for analysis or investigation

Device Classification
Risk Class
Class I
Product Type
IVD
ARTG Category
IVD
Registration Information
Start Date
August 18, 2020
Effective Date
August 18, 2020
Sponsor
Manufacturer
Country
United States of America
Address
1250 Eisenhower Place, Ann Arbor, Michigan, 48108