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HT ORIS - Operating room device management system - ARTG 480305

Access comprehensive regulatory information for HT ORIS - Operating room device management system in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 480305 and sponsored by Hospital Products Australia Pty Ltd, manufactured by Deva Group doo in Slovenia. The device registration started on February 21, 2025.

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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Class I
ARTG 480305
Class I
HT ORIS - Operating room device management system
ARTG ID: 480305
Good Name: Hospital Products Australia Pty Ltd - HT ORIS - Operating room device management system
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Intended Purpose

Hardware and Software used for integrating audiovisual devices to provide operating room (OR) staff with a single point of management to integrate/operate electromechanical/electronic medical devices of different makes during surgery. It allows the user to control, display, view, record, forward, and store medical images and videos within the operating room, making available surgical imaging data, export of perioperative imaging data from medical devices.

Device Classification
Risk Class
Class I
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
480305
Start Date
February 21, 2025
Effective Date
February 21, 2025
Manufacturer
Country
Slovenia
Address
Goriska cesta 75, Ajdovscina, 5270