Bioline Syphilis 3.0 - FDA Registration cbe251ea4b00d562a5bd9fb41742f620

Access comprehensive regulatory information for Bioline Syphilis 3.0 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID cbe251ea4b00d562a5bd9fb41742f620 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.