Pure Global

Oesophageal intubation detector, exhaled carbon dioxide, adult

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.

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TGA ARTG Official Data
Class Im
Class Im
Oesophageal intubation detector, exhaled carbon dioxide, adult
Australia TGA ARTG Registered Device
Good Name: Quest Surgical Pty Ltd - Oesophageal intubation detector, exhaled carbon dioxide, adult
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Intended Purpose

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

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
Manufacturer
Country
United States of America
Address
11300 49th Street North, Clearwater, FL, 33762