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Filter, bacteria, breathing circuit

Access comprehensive regulatory information for Filter, bacteria, breathing circuit in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Vyaire Medical Pty Ltd, manufactured by Vyaire Medical Inc also trading as Carefusion in United States of America. The device registration started on January 12, 2015.

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.

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Class IIa
Class IIa
Filter, bacteria, breathing circuit
Australia TGA ARTG Registered Device
Good Name: Vyaire Medical Pty Ltd - Filter, bacteria, breathing circuit
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Intended Purpose

A screening device installed in a gas delivery line with a membrane pore size small enough to retain bacterial and viral pathogens. This device is typically used in breathing systems and gas sampling lines to prevent the system from becoming infected and increasing the risk of cross infection of a subsequent patient. This is a disposable device.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
January 12, 2015
Effective Date
January 12, 2015
Manufacturer
Country
United States of America
Address
26125 N Riverwoods Boulevard, Mettawa, Illinois, 60045