ARTG 419351Airway, oropharyngeal, single use
ARTG ID: 419351 · Teleflex Medical Australia Pty Ltd · Teleflex Medical · Class I · Started August 22, 2023
Good Name: Teleflex Medical Australia Pty Ltd - Airway, oropharyngeal, single use
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 419351
- Start Date
- August 22, 2023
- Effective Date
- August 22, 2023
- Name
- Teleflex Medical
- Country
- Ireland
- Address
- IDA Business and Technology Park Dublin Road, Athlone, Co Westmeath
The Guedel Airway (Oropharyngeal Tube) devices are disposable devices intended to be used in hospitals and emergency situations to maintain the patency of the airway through the oral cavity and pharynx. The device prevents the tongue from obstructing airflow. This is a single-use device.
Access comprehensive regulatory information for Airway, oropharyngeal, single use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 419351 and sponsored by Teleflex Medical Australia Pty Ltd, manufactured by Teleflex Medical in Ireland. The device registration started on August 22, 2023.
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.