ARTG 447965Breathing circuit, anaesthesia, single use
ARTG ID: 447965 · GE Healthcare Australia Pty Ltd · Flexicare Medical Ltd · Class IIa · Started May 07, 2024
Good Name: GE Healthcare Australia Pty Ltd - Breathing circuit, anaesthesia, single use
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 447965
- Start Date
- May 07, 2024
- Effective Date
- May 07, 2024
- Country
- United Kingdom
- Address
- Cynon Valley Business Park, Mountain Ash, CF45 4ER
A non-sterile assembly of devices designed to conduct medical gases from the fresh gas supply outlet of an anaesthesia unit/workstation to the patient, typically connecting the patient, a ventilator/ventilation bag, carbon dioxide (CO2) absorber, and a monitor. It typically includes both an inhalation and exhalation route and consists of breathing tubes, a ventilation and/or reservoir bag(s), a Y-piece, connectors/adaptors, and gas sampling ports. The absorber, a one-way directional valve, and adjustable pressure limiting (APL) valve are also devices typically employed in the circuit but may not be a part of this device. This is a single-use device.
Access comprehensive regulatory information for Breathing circuit, anaesthesia, single use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 447965 and sponsored by GE Healthcare Australia Pty Ltd, manufactured by Flexicare Medical Ltd in United Kingdom. The device registration started on May 07, 2024.
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.