Reinforced endotracheal tube, single-use - ARTG 462118
Access comprehensive regulatory information for Reinforced endotracheal tube, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 462118 and sponsored by Airlife Australia Holdings Pty Ltd, manufactured by Well Lead Medical Co Ltd in China. The device registration started on September 10, 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.
The Reinforced Endotracheal Tube is used in general anaesthesia, intensive care and emergency medicine for airway management and mechanical ventilation. The tube is inserted into a patient's trachea through the patient's nose or mouth in order to ensure that the airway is not closed off and that air is able to reach the lungs.