Australia TGA ARTG record

Heel stirrup

Australia TGA ARTG Registered Device · Steris Australia Pty Ltd · Allen Medical Systems Inc · Class I · Started August 23, 2023

Good Name: Steris Australia Pty Ltd - Heel stirrup

Device classification

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

Registration information

Start Date: August 23, 2023
Effective Date: August 23, 2023

Sponsor

Name: Steris Australia Pty Ltd

Manufacturer

Name: Allen Medical Systems Inc
Country: United States of America
Address: 100 Discovery Way, Acton, MA, 01720

Intended purpose

The Stirrup is designed to position and support the patient’s foot, lower leg and upper leg in a variety of surgical procedures including, but not limited to gynecology, urology, laparoscopy, general and robotic surgery. These devices are intended to be used by healthcare professionals within the Operating Room setting.

About this record

Access comprehensive regulatory information for Heel stirrup in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Steris Australia Pty Ltd, manufactured by Allen Medical Systems Inc in United States of America. The device registration started on August 23, 2023.

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.