Pure Global

Resuscitator, pulmonary, manual, single use - ARTG 312514

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 registered under ARTG number 312514 and 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.

Free Database
Powered by Pure Global AI
TGA ARTG Official Data
Class IIa
ARTG 312514
Class IIa
Resuscitator, pulmonary, manual, single use
ARTG ID: 312514
Good Name: Laerdal Pty Ltd - Resuscitator, pulmonary, manual, single use
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Intended Purpose

To manually ventilate an infant, adult or child.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
312514
Start Date
December 14, 2018
Effective Date
December 14, 2018
Sponsor
Manufacturer
Country
Norway
Address
Tanke Svilangsgate 30, Stavanger, 4002