Pure Global

Ventilator, software

Access comprehensive regulatory information for Ventilator, software in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Resmed Pty Ltd, manufactured by ResMed Corp in United States of America. The device registration started on September 10, 2021.

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
Class IIb
Ventilator, software
Australia TGA ARTG Registered Device
Good Name: Resmed Pty Ltd - Ventilator, software
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Intended Purpose

Software for data analysis and management of compatible ResMed Flow Generator and Respiratory Care devices. Data collection and management capabilities provide an adjunct for a patient compliance management.

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
September 10, 2021
Effective Date
September 10, 2021
Sponsor
Manufacturer
Country
United States of America
Address
9001 Spectrum Center Blvd, San Diego, CA, 92123