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Home CPAP unit - ARTG 483185

Access comprehensive regulatory information for Home CPAP unit in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 483185 and sponsored by Resmed Pty Ltd, manufactured by ResMed Corp in United States of America. The device registration started on March 19, 2025.

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 I
ARTG 483185
Class I
Home CPAP unit
ARTG ID: 483185
Good Name: Resmed Pty Ltd - Home CPAP unit
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Intended Purpose

The Comfort Match software product provides recommendations for comfort settings for patients using compatible ResMed Positive Airway Pressure (PAP) therapy devices. Comfort Match is an optional tool which can be used to recommend specific comfort settings for individual patients.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
483185
Start Date
March 19, 2025
Effective Date
March 19, 2025
Sponsor
Manufacturer
Country
United States of America
Address
9001 Spectrum Center Blvd, San Diego, CA, 92123