Endoscopic insufflation tubing set
ARTG ID: 278525 · Steris Australia Pty Ltd · United States Endoscopy Group Inc also T/a US Endoscopy · Class IIa · Started August 01, 2016
Good Name: Steris Australia Pty Ltd - Endoscopic insufflation tubing set
- Risk Class
- Class IIa
- Product Type
- Procedure Pack
- ARTG Category
- General
- ARTG ID
- 278525
- Start Date
- August 01, 2016
- Effective Date
- August 01, 2016
- Country
- United States of America
- Address
- 5976 Heisley Road, MENTOR, Ohio, 44060
An endoscopic tubing set is intended to administer medical gases from an insufflator to the water/air channel of an endoscope for insufflation during an endoscopic procedure. The insufflator is supplied separately and is an electrically powered device.
Access comprehensive regulatory information for Endoscopic insufflation tubing set in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 278525 and sponsored by Steris Australia Pty Ltd, manufactured by United States Endoscopy Group Inc also T/a US Endoscopy in United States of America. The device registration started on August 01, 2016.
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.