Pure Global

Submucosal lift solution - ARTG 463725

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.

Free Database
Powered by Pure Global AI
TGA ARTG Official Data
Class IIb
ARTG 463725
Class IIb
Submucosal lift solution
ARTG ID: 463725
Good Name: Steris Australia Pty Ltd - Submucosal lift solution
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
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.

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
Manufacturer
Country
United States of America
Address
5976 Heisley Road, MENTOR, Ohio, 44060