Aerogen Pro USB Controller Starter Kit - FDA Registration d3b559b6786947c31a8829c05ea19b14

Access comprehensive regulatory information for Aerogen Pro USB Controller Starter Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d3b559b6786947c31a8829c05ea19b14 and manufactured by Aerogen Ltd., M&M Qualtech Ltd.. The device was registered on September 20, 2022.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.