Australia TGA ARTG recordAirway, oropharyngeal, single use
Australia TGA ARTG Registered Device · Bosco Medical Australia · Ningbo Luke Medical Devices Co Ltd · Class Is · Started August 30, 2021
Good Name: Bosco Medical Australia - Airway, oropharyngeal, single use
- Risk Class
- Class Is
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- August 30, 2021
- Effective Date
- August 30, 2021
- Country
- China
- Address
- Gujiayan Yangming Road, Yuyao City, Zhejiang Province, 315400
Guedel airways intended to maintain the patency of the respiratory passages through the oral cavity and pharynx.
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.