AIRFLOW MAX Introduction Kit - FDA Registration 5ae72e086b83e79f055efa4996b1f794

Access comprehensive regulatory information for AIRFLOW MAX Introduction Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5ae72e086b83e79f055efa4996b1f794 and manufactured by E.M.S Electro Medical System S.A. The device was registered on July 06, 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.