NeuMoDx™ LDT - FDA Registration ce3382ea1b69d05f22db4a53e4b09775

Access comprehensive regulatory information for NeuMoDx™ LDT in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ce3382ea1b69d05f22db4a53e4b09775 and manufactured by NeuMoDx Molecular, Inc.. The device was registered on February 10, 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.