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Filter, <specify> - ARTG 466265

Access comprehensive regulatory information for Filter, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 466265 and sponsored by Philips Electronics Australia Ltd, manufactured by Respironics Inc in United States of America. The device registration started on October 29, 2024.

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 I
ARTG 466265
Class I
Filter, <specify>
ARTG ID: 466265
Good Name: Philips Electronics Australia Ltd - Filter, <specify>
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Intended Purpose

The Particulate Filter is intended to be used as an accessory for the Trilogy Evo Platform (Trilogy Evo, Trilogy Evo O2, and Trilogy EV300) to prevent dirt and dust.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
466265
Start Date
October 29, 2024
Effective Date
October 29, 2024
Manufacturer
Country
United States of America
Address
1001 Murry Ridge Lane, Murrysville, PA, 15668-8550