ARCHITECT 2nd Generation Testosterone Reagent Kit - FDA Registration 3d0075c2a8a0bac2bb262d364c772532

Access comprehensive regulatory information for ARCHITECT 2nd Generation Testosterone Reagent Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3d0075c2a8a0bac2bb262d364c772532 and manufactured by Axis-Shield Diagnostics Limited. The device was registered on October 28, 2021.

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.