Australia flagARTG 120792

MRI-patient physiologic monitoring system

ARTG ID: 120792 · Intermed Medical Pty Ltd · Schiller Medical · Class IIb · Started July 22, 2005

Good Name: Intermed Medical Pty Ltd - MRI-patient physiologic monitoring system

Device classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration information
ARTG ID
120792
Start Date
July 22, 2005
Effective Date
July 22, 2005
Sponsor
Manufacturer
Country
France
Address
4 Rue Louis Pasteur, Wisssembourg Cedex, 67160
Intended purpose

The MagLife unit, utilizes built-in functions, and collects several monitoring parameters and displays these by the patient beside in an MRI environment. The monitoring parameters can be, e.g. ECG, BP, temperature, cardiac output or respiration gases, pulse oximetry, capnography

About this record

Access comprehensive regulatory information for MRI-patient physiologic monitoring system in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 120792 and sponsored by Intermed Medical Pty Ltd, manufactured by Schiller Medical in France. The device registration started on July 22, 2005.

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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