Dengue IgG/IgM Antibody Test - FDA Registration a15c4b87878336610ac4e11b2b3a50a8

Access comprehensive regulatory information for Dengue IgG/IgM Antibody Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a15c4b87878336610ac4e11b2b3a50a8 and manufactured by Humasis Co.,Ltd. The device was registered on November 21, 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.