Australia flagARTG 476389

Carbon dioxide cuvette, single-use

ARTG ID: 476389 · Airlife Australia Holdings Pty Ltd · Respironics Novametrix LLC · Class IIa · Started January 22, 2025

Good Name: Airlife Australia Holdings Pty Ltd - Carbon dioxide cuvette, single-use

Device classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration information
ARTG ID
476389
Start Date
January 22, 2025
Effective Date
January 22, 2025
Sponsor
Manufacturer
Country
United States of America
Address
3000 Minuteman Road, Andover, MA, 01810
Intended purpose

For monitoring Pediatric/Adult patients with endotracheal tube size greater than 4.0mm with the CAPNOSTAT CO2 sensor.

About this record

Access comprehensive regulatory information for Carbon dioxide cuvette, 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 476389 and sponsored by Airlife Australia Holdings Pty Ltd, manufactured by Respironics Novametrix LLC in United States of America. The device registration started on January 22, 2025.

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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