Australia TGA ARTG recordReinforced endotracheal tube, single-use
Australia TGA ARTG Registered Device · Genesis Airway Innovations Pty Ltd · Hangzhou Formed Medical Devices Co Ltd · Class IIa · Started July 23, 2020
Good Name: Genesis Airway Innovations Pty Ltd - Reinforced endotracheal tube, single-use
- Risk Class
- Class IIa
- Product Type
- Medical device system
- ARTG Category
- General
- Start Date
- July 23, 2020
- Effective Date
- July 23, 2020
- Country
- China
- Address
- Building 3 No 292 Gonghe North Road Xindeng Town Fuyang District, Hangzhou, 311404
A reinforced endortracheal tube system 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.
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 IIa is sponsored by Genesis Airway Innovations Pty Ltd, manufactured by Hangzhou Formed Medical Devices Co Ltd in China. The device registration started on July 23, 2020.
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.