Australia TGA ARTG recordResuscitator, pulmonary, manual, single use
Australia TGA ARTG Registered Device · Laerdal Pty Ltd · Laerdal Medical AS · Class IIa · Started December 14, 2018
Good Name: Laerdal Pty Ltd - Resuscitator, pulmonary, manual, single use
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- December 14, 2018
- Effective Date
- December 14, 2018
- Name
- Laerdal Pty Ltd
- Country
- Norway
- Address
- Tanke Svilangsgate 30, Stavanger, 4002
To manually ventilate an infant, adult or child.
Access comprehensive regulatory information for Resuscitator, pulmonary, manual, single use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Laerdal Pty Ltd, manufactured by Laerdal Medical AS in Norway. The device registration started on December 14, 2018.
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.