Australia TGA ARTG recordPhysiologic-monitoring defibrillation system
Australia TGA ARTG Registered Device · Philips Electronics Australia Ltd · Schiller AG · Class IIb · Started April 20, 2021
Good Name: Philips Electronics Australia Ltd - Physiologic-monitoring defibrillation system
- Risk Class
- Class IIb
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- April 20, 2021
- Effective Date
- April 20, 2021
- Name
- Schiller AG
- Country
- Switzerland
- Address
- Altgasse 68, Baar, 6341
A defibrillator that can deliver a shock in automatic, manual or pacemaker mode. The device can be used for patient monitoring without alarms and with the following optional features: 3-wire and 4-wire ECG cable (without alarm handling), SpO2 sensor (without alarm handling). The device is for use by professional persons who are trained in basic life support and defibrillation or advanced life support. The device is intended for single patient use.
Access comprehensive regulatory information for Physiologic-monitoring defibrillation system in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Philips Electronics Australia Ltd, manufactured by Schiller AG in Switzerland. The device registration started on April 20, 2021.
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.