Valve, <specify> - ARTG 389887

Access comprehensive regulatory information for Valve, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 389887 and sponsored by Air Liquide Healthcare Pty Ltd, manufactured by Parker Hannifin Corp Precision Fluidics Division in United States of America. The device registration started on June 09, 2022.

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.