Australia TGA ARTG recordTube/mask breathing circuit connector, non-sterile, single-use
Australia TGA ARTG Registered Device · Device Technologies Australia Pty Ltd · Vadi Medical Technology Co Ltd Yangmei · Class IIa · Started May 16, 2022
Good Name: Device Technologies Australia Pty Ltd - Tube/mask breathing circuit connector, non-sterile, single-use
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- May 16, 2022
- Effective Date
- May 16, 2022
- Country
- Taiwan
- Address
- No 198 Lane 298 Huandong Road, ZhongShan Village Yangmei District, Taoyuan City, 32665
A connector intended to provide connection between two devices in order to enable the delivery of respiratory gases to the patient.
Access comprehensive regulatory information for Tube/mask breathing circuit connector, non-sterile, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Device Technologies Australia Pty Ltd, manufactured by Vadi Medical Technology Co Ltd Yangmei in Taiwan. The device registration started on May 16, 2022.
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.