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Airway, oropharyngeal, single use - ARTG 419351

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.

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TGA ARTG Official Data
Class I
ARTG 419351
Class I
Airway, oropharyngeal, single use
ARTG ID: 419351
Good Name: Teleflex Medical Australia Pty Ltd - Airway, oropharyngeal, single use
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Intended Purpose

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.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
419351
Start Date
August 22, 2023
Effective Date
August 22, 2023
Manufacturer
Country
Ireland
Address
IDA Business and Technology Park Dublin Road, Athlone, Co Westmeath