Xpert Xpress Flu/RSV - FDA Registration 5177db1c396c780824ffcc79f818728f

Access comprehensive regulatory information for Xpert Xpress Flu/RSV in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5177db1c396c780824ffcc79f818728f and manufactured by Cepheid. The device was registered on November 18, 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.