Xpert Xpress SARS-CoV-2 - FDA Registration 31ab1bb641d22b3dc4fcbc6253946685

Access comprehensive regulatory information for Xpert Xpress SARS-CoV-2 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 31ab1bb641d22b3dc4fcbc6253946685 and manufactured by Cepheid. The device was registered on April 01, 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.