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Cardiopulmonary resuscitation feedback device

Access comprehensive regulatory information for Cardiopulmonary resuscitation feedback device in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Laerdal Pty Ltd, manufactured by Laerdal Medical AS in Norway. The device registration started on June 27, 2016.

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
Class I
Cardiopulmonary resuscitation feedback device
Australia TGA ARTG Registered Device
Good Name: Laerdal Pty Ltd - Cardiopulmonary resuscitation feedback device
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Intended Purpose

A small, lightweight device powered by replaceable batteries intended for use by responders who have been trained in CPR and use of the CPR meter.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
June 27, 2016
Effective Date
June 27, 2016
Sponsor
Manufacturer
Country
Norway
Address
Tanke Svilangsgate 30, Stavanger, 4002