Fungal infectious disease IVDs - ARTG 383588
Access comprehensive regulatory information for Fungal infectious disease IVDs in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 383588 and sponsored by R-Biopharm Pty Ltd, manufactured by Diesse Diagnostica Senese SPA in Italy. The device registration started on February 07, 2022.
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.
Intended to be used in testing to provide information about infection with or exposure to yeast and fungal diseases

