Aerogen Pro USB Controller Starter Kit
MyanmarAerogenAerogen Ltd., M&M Qualtech Ltd.Registered September 20, 2022
VerifiedFDA Myanmar · official registry
Device classification
- Brand Name
- Aerogen
Registration information
- Analysis ID
- d3b559b6786947c31a8829c05ea19b14
- Registration Date
- September 20, 2022
Manufacturer
Authorized Representative
About this record
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.