Australia TGA ARTG recordInspiratory line humidification chamber, single-use
Australia TGA ARTG Registered Device · Fisher & Paykel Healthcare Pty Ltd · Fisher & Paykel Healthcare Ltd · Class IIa · Started September 15, 2023
Good Name: Fisher & Paykel Healthcare Pty Ltd - Inspiratory line humidification chamber, single-use
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- September 15, 2023
- Effective Date
- September 15, 2023
- Country
- New Zealand
- Address
- 15 Maurice Paykel Place, East Tamaki, Auckland , 2013
Humidification chamber that stores and allows heating of water for the humidification of respiratory gases.
Access comprehensive regulatory information for Inspiratory line humidification chamber, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Fisher & Paykel Healthcare Pty Ltd, manufactured by Fisher & Paykel Healthcare Ltd in New Zealand. The device registration started on September 15, 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.