ARTG 379573Cannula, nasal, carbon dioxide sampling
ARTG ID: 379573 · Philips Electronics Australia Ltd · Philips Medical Systems · Class IIa · Started November 30, 2021
Good Name: Philips Electronics Australia Ltd - Cannula, nasal, carbon dioxide sampling
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 379573
- Start Date
- November 30, 2021
- Effective Date
- November 30, 2021
- Country
- United States of America
- Address
- 3000 Minuteman Road, Andover, Massachusetts, 01810-1099
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.
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.