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Basic endotracheal tube, single-use - ARTG 340039

Access comprehensive regulatory information for Basic endotracheal tube, 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 340039 and 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.

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TGA ARTG Official Data
Class IIa
ARTG 340039
Class IIa
Basic endotracheal tube, single-use
ARTG ID: 340039
Good Name: Genesis Airway Innovations Pty Ltd - Basic endotracheal tube, single-use
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Intended Purpose

An endotracheal 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

Device Classification
Risk Class
Class IIa
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
340039
Start Date
July 23, 2020
Effective Date
July 23, 2020
Manufacturer
Country
China
Address
Building 3 No 292 Gonghe North Road Xindeng Town Fuyang District, Hangzhou, 311404