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Oesophageal intubation detector, exhaled carbon dioxide, adult - ARTG 452166

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 I is registered under ARTG number 452166 and sponsored by Cardinal Health Australia 503 Pty Ltd, manufactured by Cardinal Health 200 LLC in United States of America. The device registration started on June 14, 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.

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TGA ARTG Official Data
Class I
ARTG 452166
Class I
Oesophageal intubation detector, exhaled carbon dioxide, adult
ARTG ID: 452166
Good Name: Cardinal Health Australia 503 Pty Ltd - Oesophageal intubation detector, exhaled carbon dioxide, adult
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Intended Purpose

An accessory to a gastric tube to assist in the determination of proper tube placement by detecting carbon dioxide (CO2) in the gas present at the tip of the tube. This device is used to assist verification of tube placement during nasal/oral gastric tube placement in adults and helps avoid inadvertent tracheal placement.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
452166
Start Date
June 14, 2024
Effective Date
June 14, 2024
Manufacturer
Country
United States of America
Address
3651 Birchwood Drive, Waukegan, Illinois, 60085