ARCHITECT - FDA Registration b5451ea912f6515f1bddbcf28999112f

Access comprehensive regulatory information for ARCHITECT in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b5451ea912f6515f1bddbcf28999112f and manufactured by Fujirebio Diagnostics Inc.,. The device was registered on May 26, 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.