Australia TGA ARTG recordVadi Expiratory Heated Filter System - Air filter
Australia TGA ARTG Registered Device · Bellavista Medical ANZ Pty Ltd · Vadi Medical Technology Co Ltd Yangmei · Class I · Started March 22, 2019
Good Name: Bellavista Medical ANZ Pty Ltd - Vadi Expiratory Heated Filter System - Air filter
- Risk Class
- Class I
- Product Type
- Medical device system
- ARTG Category
- General
- Start Date
- March 22, 2019
- Effective Date
- March 22, 2019
- Country
- Taiwan
- Address
- 5F-2 No 492-19 Sec 1 Wan Shou Rd Kwei Shan Hsiang, Taoyuan, Hsien
The Vadi Heated Expiratory Filter System is a large surface area reusable or disposable respiratory filter system, that heats the expiratory filter to reduce/remove any condensate moisture build up on the filter's surface, which would normally cause unwanted expiratory breathing resistance, removes 99.99% contaminates, and allows continued uninterrupted circuit and ventilator use for up to 14 days, reducing staff and patient cross-contamination, and significantly reducing de-recruitment of patients respiratory alveoli.
Access comprehensive regulatory information for Vadi Expiratory Heated Filter System - Air filter in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Bellavista Medical ANZ Pty Ltd, manufactured by Vadi Medical Technology Co Ltd Yangmei in Taiwan. The device registration started on March 22, 2019.
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.