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Oesophageal intubation detector, exhaled carbon dioxide, adult - ARTG 463405

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 463405 and sponsored by Fisher & Paykel Healthcare Pty Ltd, manufactured by Fisher & Paykel Healthcare Ltd in New Zealand. The device registration started on October 02, 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 463405
Class I
Oesophageal intubation detector, exhaled carbon dioxide, adult
ARTG ID: 463405
Good Name: Fisher & Paykel Healthcare Pty Ltd - Oesophageal intubation detector, exhaled carbon dioxide, adult
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Intended Purpose

To detect exhaled CO2.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
463405
Start Date
October 02, 2024
Effective Date
October 02, 2024
Manufacturer
Country
New Zealand
Address
15 Maurice Paykel Place, East Tamaki, Auckland , 2013