Syphilis RPR Test - FDA Registration 564b4049b420dc6782c03fdc6a609890

Access comprehensive regulatory information for Syphilis RPR Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 564b4049b420dc6782c03fdc6a609890 and manufactured by Gesellschaft für Biochemica und Diagnostica mbH. The device was registered on September 08, 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.