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Spirometer, diagnostic

Australia TGA ARTG Registered Device · MGC Diagnostics Australia Pty Ltd · MediSoft SA · Class IIa · Started February 26, 2008

Good Name: MGC Diagnostics Australia Pty Ltd - Spirometer, diagnostic

Device classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration information
Start Date
February 26, 2008
Effective Date
February 26, 2008
Sponsor
Manufacturer
Country
Belgium
Address
1 PAE de Sorinnes Route de la voie cuivree, Dinant, Sorinnes, 5503
Intended purpose

A device intended to measure lung air volume and airflow rate for pulmonary disease diagnosis and screening. These measurements provide information about a patient's pulmonary function which may be compared with normal values or the patient's former values.

About this record

Access comprehensive regulatory information for Spirometer, diagnostic in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by MGC Diagnostics Australia Pty Ltd, manufactured by MediSoft SA in Belgium. The device registration started on February 26, 2008.

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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