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Endoscopic insufflation tubing set - ARTG 278525

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.

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TGA ARTG Official Data
Class IIa
ARTG 278525
Class IIa
Endoscopic insufflation tubing set
ARTG ID: 278525
Good Name: Steris Australia Pty Ltd - Endoscopic insufflation tubing set
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Intended Purpose

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.

Device Classification
Risk Class
Class IIa
Product Type
Procedure Pack
ARTG Category
General
Registration Information
ARTG ID
278525
Start Date
August 01, 2016
Effective Date
August 01, 2016
Manufacturer
Country
United States of America
Address
5976 Heisley Road, MENTOR, Ohio, 44060