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Sanofi Pasteur Inc

Manufacturer • United States of America · 1 device on the TGA ARTG · 1 device class · Mar 07, 2019 – Mar 07, 2019

1
Total Devices
1
Device Classes
2019
Earliest
2019
Latest
Recent device registrations
Latest 10 TGA ARTG device registrations
Medicine administration kit, percutaneous, medicated, single-use
Class IIaMar 07, 2019
Sponsor: Sanofi-Aventis Australia Pty Ltd
Risk class distribution
Devices by risk class
Class IIa
1
100.0% of total
About this profile

Explore comprehensive manufacturer profile for Sanofi Pasteur Inc through Pure Global AI's free Australia TGA ARTG medical device database. This company has manufactured 1 medical device registered with TGA ARTG across 1 device class. This manufacturer is based in United States of America. Their registration history spans from Mar 07, 2019 to Mar 07, 2019.

This page provides detailed insights including recent device registrations, risk class distribution (Class IIa: 1), and complete regulatory information 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.

Free Manufacturer ProfilePowered by Pure Global AI1 Devices1 Device Classes