ARTG 463725

Submucosal lift solution

ARTG ID: 463725 · Steris Australia Pty Ltd · United States Endoscopy Group Inc also T/a US Endoscopy · Class IIb · Started October 07, 2024

Good Name: Steris Australia Pty Ltd - Submucosal lift solution

Device classification

Risk Class: Class IIb
Product Type: Single Device Product
ARTG Category: General

Registration information

ARTG ID: 463725
Start Date: October 07, 2024
Effective Date: October 07, 2024

Sponsor

Name: Steris Australia Pty Ltd

Manufacturer

Name: United States Endoscopy Group Inc also T/a US Endoscopy
Country: United States of America
Address: 5976 Heisley Road, MENTOR, Ohio, 44060

Intended purpose

A submucosal lifting agent is intended for use in gastrointestinal endoscopic procedures for submucosal lift of polyps, adenomas, early-stage cancers or other gastrointestinal mucosal lesions prior to excision with a snare or endoscopic device.

About this record

Access comprehensive regulatory information for Submucosal lift solution in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 463725 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 October 07, 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.