Pure Global

Spirometer, diagnostic

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 Intermed Medical Pty Ltd, manufactured by Schiller AG in Switzerland. The device registration started on February 08, 2018.

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
Spirometer, diagnostic
Australia TGA ARTG Registered Device
Good Name: Intermed Medical Pty Ltd - Spirometer, diagnostic
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Intended Purpose

This is a device that is intended to be used to measure lung air volume and airflow rate for pulmonary disease diagnosis and screening. The flow/volume measurement, in- and expiratory vital capacity, partial volumes, second-volume FEV1, maximum voluntary ventilation MVV, peak-flow and more than 40 sub-parameters These measurements provide information about a patient's pulmonary function which may be compared with normal values or the patient's former values.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
February 08, 2018
Effective Date
February 08, 2018
Manufacturer
Country
Switzerland
Address
Altgasse 68, Baar, 6341