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Cytomegalovirus (Human herpesvirus 5) IVDs - ARTG 223978

Access comprehensive regulatory information for Cytomegalovirus (Human herpesvirus 5) IVDs in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 223978 and sponsored by R-Biopharm Pty Ltd, manufactured by Diesse Diagnostica Senese SPA in Italy. The device registration started on June 02, 2014.

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 IIb
ARTG 223978
Class IIb
Cytomegalovirus (Human herpesvirus 5) IVDs
ARTG ID: 223978
Good Name: R-Biopharm Pty Ltd - Cytomegalovirus (Human herpesvirus 5) IVDs
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Intended Purpose

IVDs that are intended to be used in testing to provide information about infection with or exposure to Cytomegalovirus (CMV)

Device Classification
Risk Class
Class IIb
Product Type
IVD
ARTG Category
IVD
Registration Information
ARTG ID
223978
Start Date
June 02, 2014
Effective Date
June 02, 2014
Manufacturer
Country
Italy
Address
Strada Dei Laghi 39, Monteriggioni, 53035