S. Typhi/Paratyphi Ag Rapid Test - FDA Registration 8096b731e041fdf162d53af7ce2890dc

Access comprehensive regulatory information for S. Typhi/Paratyphi Ag Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8096b731e041fdf162d53af7ce2890dc and manufactured by CTK Biotech. Inc.. The device was registered on December 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.