Australia TGA ARTG record

Oesophageal intubation detector, exhaled carbon dioxide, adult

Australia TGA ARTG Registered Device · Quest Surgical Pty Ltd · Mercury Medical · Class Im · Started April 14, 2020

Good Name: Quest Surgical Pty Ltd - Oesophageal intubation detector, exhaled carbon dioxide, adult

Device classification

Risk Class: Class Im
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: April 14, 2020
Effective Date: April 14, 2020

Sponsor

Name: Quest Surgical Pty Ltd

Manufacturer

Name: Mercury Medical
Country: United States of America
Address: 11300 49th Street North, Clearwater, FL, 33762

Intended purpose

Disposable Device to Measure/Detect exhaled gas during oesophageal intubation for patients over 15kg

About this record

Access comprehensive regulatory information for Oesophageal intubation detector, exhaled carbon dioxide, adult in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class Im is sponsored by Quest Surgical Pty Ltd, manufactured by Mercury Medical in United States of America. The device registration started on April 14, 2020.

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.