ARTG 281880Specimen receptacle IVDs
ARTG ID: 281880 · Qiagen Pty Ltd · QIAGEN Sciences LLC · Class I · Started October 28, 2016
Good Name: Qiagen Pty Ltd - Specimen receptacle IVDs
- Risk Class
- Class I
- Product Type
- IVD
- ARTG Category
- IVD
- ARTG ID
- 281880
- Start Date
- October 28, 2016
- Effective Date
- October 28, 2016
- Name
- Qiagen Pty Ltd
- Country
- United States of America
- Address
- 19300 Germantown Road, Germantown, MD, 20874
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
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 registered under ARTG number 281880 and sponsored by Qiagen Pty Ltd, manufactured by QIAGEN Sciences LLC in United States of America. The device registration started on October 28, 2016.
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.