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Cannula, nasal, carbon dioxide sampling - ARTG 379573

Access comprehensive regulatory information for Cannula, nasal, carbon dioxide sampling in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 379573 and sponsored by Philips Electronics Australia Ltd, manufactured by Philips Medical Systems in United States of America. The device registration started on November 30, 2021.

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 IIa
ARTG 379573
Class IIa
Cannula, nasal, carbon dioxide sampling
ARTG ID: 379573
Good Name: Philips Electronics Australia Ltd - Cannula, nasal, carbon dioxide sampling
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Intended Purpose

Intended to sample CO2 and administer supplemental oxygen, for patients who can wear a 60 fr. bite block, during upper endoscopy type procedures. The set is intended for single patient use only.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
379573
Start Date
November 30, 2021
Effective Date
November 30, 2021
Manufacturer
Country
United States of America
Address
3000 Minuteman Road, Andover, Massachusetts, 01810-1099