Carbon dioxide cuvette, single-use - ARTG 476389

Access comprehensive regulatory information for Carbon dioxide cuvette, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 476389 and sponsored by Airlife Australia Holdings Pty Ltd, manufactured by Respironics Novametrix LLC in United States of America. The device registration started on January 22, 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.