Australia TGA ARTG record

Endoscopic forceps, biopsy, flexible

Australia TGA ARTG Registered Device · Medtronic Australasia Pty Ltd · Endo-Therapeutics Inc · Class Is · Started August 21, 2007

Good Name: Medtronic Australasia Pty Ltd - Endoscopic forceps, biopsy, flexible

Device classification

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

Registration information

Start Date: August 21, 2007
Effective Date: August 21, 2007

Sponsor

Name: Medtronic Australasia Pty Ltd

Manufacturer

Name: Endo-Therapeutics Inc
Country: United States of America
Address: 15251 Roosevelt Boulevard 204, Clearwater, FL, 33760

Intended purpose

An endoscopic instrument intended to be used to perform through a compatible endoscope. It is introduced into the body cavity through an artificial orifice of the body or the working channel of the endoscope. This device is supplied sterile.

About this record

Access comprehensive regulatory information for Endoscopic forceps, biopsy, flexible in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class Is is sponsored by Medtronic Australasia Pty Ltd, manufactured by Endo-Therapeutics Inc in United States of America. The device registration started on August 21, 2007.

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.