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Airway, oropharyngeal, single use

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 Is is sponsored by Bosco Medical Australia, manufactured by Ningbo Luke Medical Devices Co Ltd in China. The device registration started on August 30, 2021.

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 Is
Class Is
Airway, oropharyngeal, single use
Australia TGA ARTG Registered Device
Good Name: Bosco Medical Australia - Airway, oropharyngeal, single use
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Intended Purpose

Guedel airways intended to maintain the patency of the respiratory passages through the oral cavity and pharynx.

Device Classification
Risk Class
Class Is
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
August 30, 2021
Effective Date
August 30, 2021
Manufacturer
Country
China
Address
Gujiayan Yangming Road, Yuyao City, Zhejiang Province, 315400