Australia TGA ARTG record

Medical device electrical cable, general purpose

Australia TGA ARTG Registered Device · Philips Electronics Australia Ltd · Respironics Inc · Class I · Started April 05, 2023

Good Name: Philips Electronics Australia Ltd - Medical device electrical cable, general purpose

Device classification

Risk Class: Class I
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: April 05, 2023
Effective Date: April 05, 2023

Sponsor

Name: Philips Electronics Australia Ltd

Manufacturer

Name: Respironics Inc
Country: United States of America
Address: 1001 Murry Ridge Lane, Murrysville, PA, 15668-8550

Intended purpose

An accessory used to operate Philips Respironics' CPAP and BiPAP systems when AC power is not available.

About this record

Access comprehensive regulatory information for Medical device electrical cable, general purpose in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Philips Electronics Australia Ltd, manufactured by Respironics Inc in United States of America. The device registration started on April 05, 2023.

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.