Australia TGA ARTG record

Ventilator, software

Australia TGA ARTG Registered Device · Resmed Pty Ltd · ResMed Corp · Class IIb · Started September 10, 2021

Good Name: Resmed Pty Ltd - Ventilator, software

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

Name: Resmed Pty Ltd

Manufacturer

Name: ResMed Corp
Country: United States of America
Address: 9001 Spectrum Center Blvd, San Diego, CA, 92123

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.

About this record

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.