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Instrument/analyser IVDs

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 Abbott Rapid Diagnostics Pty Ltd, manufactured by Abbott Rapid Diagnostics Jena GmbH in Germany. The device registration started on July 17, 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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Class I
Class I
Instrument/analyser IVDs
Australia TGA ARTG Registered Device
Good Name: Abbott Rapid Diagnostics Pty Ltd - Instrument/analyser IVDs
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Intended Purpose

The m-PIMAโ„ข Analyser is a portable automated bench-top analyser for processing m-PIMAโ„ข test cartridges.

Device Classification
Risk Class
Class I
Product Type
IVD
ARTG Category
IVD-Export
Registration Information
Start Date
July 17, 2020
Effective Date
July 17, 2020
Manufacturer
Country
Germany
Address
Orlaweg 1, Jena, Germany, 07743