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Fungal infectious disease IVDs

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 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.

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Class IIa
Class IIa
Fungal infectious disease IVDs
Australia TGA ARTG Registered Device
Good Name: R-Biopharm Pty Ltd - Fungal infectious disease IVDs
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Intended Purpose

Intended to be used in testing to provide information about infection with or exposure to yeast and fungal diseases

Device Classification
Risk Class
Class IIa
Product Type
IVD
ARTG Category
IVD
Registration Information
Start Date
February 07, 2022
Effective Date
February 07, 2022
Manufacturer
Country
Italy
Address
Strada Dei Laghi 39, Monteriggioni, 53035