Alpha-Fetoprotein Test Kit (Rate Scattering Turbidimetric Method) - FDA Registration b80710296ac85879846fa3138e62eb1f

Access comprehensive regulatory information for Alpha-Fetoprotein Test Kit (Rate Scattering Turbidimetric Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b80710296ac85879846fa3138e62eb1f and manufactured by Shijiazhuang Hipro Biotechnology Co.,ltd. The device was registered on August 11, 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.