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Heel stirrup

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.

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TGA ARTG Official Data
Class I
Class I
Heel stirrup
Australia TGA ARTG Registered Device
Good Name: Steris Australia Pty Ltd - Heel stirrup
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Intended Purpose

The Stirrup is designed to position and support the patientโ€™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.

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
Manufacturer
Country
United States of America
Address
100 Discovery Way, Acton, MA, 01720