Bioline HIV 1/2 3.0 - FDA Registration 4633faa0591c15e50283b64dfb07f184

Access comprehensive regulatory information for Bioline HIV 1/2 3.0 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4633faa0591c15e50283b64dfb07f184 and manufactured by Abbott Diagnostics Korea Inc.. The device was registered on March 25, 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.