H.Pylori Antigen Test Card - FDA Registration 9e4e4379f2f66be09ee66e09e6850d8f

Access comprehensive regulatory information for H.Pylori Antigen Test Card in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9e4e4379f2f66be09ee66e09e6850d8f and manufactured by LumiQuick Diagnostics, Inc.. The device was registered on August 19, 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.