MaxLINE Dengue Antigen & Antibody Duo Test - FDA Registration 94686aaf02adae96967a07dcd7dc44f6

Access comprehensive regulatory information for MaxLINE Dengue Antigen & Antibody Duo Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 94686aaf02adae96967a07dcd7dc44f6 and manufactured by Avecon Healthcare Pvt. Ltd.. The device was registered on August 17, 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.