Myanmar FDA registration d3b559b6786947c31a8829c05ea19b14

Aerogen Pro USB Controller Starter Kit

Myanmar·Aerogen·Aerogen Ltd., M&M Qualtech Ltd.·Registered September 20, 2022

Device classification

Brand Name: Aerogen

Registration information

Analysis ID: d3b559b6786947c31a8829c05ea19b14
Registration Date: September 20, 2022

Manufacturer

Name: Aerogen Ltd., M&M Qualtech Ltd.

Authorized Representative

Name: ADVAMED MEDICAL INNOVATION COMPANY LIMITED

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.