Alpha-Fetoprotein Test Kit ( Rate Scattering Turbidimetric Method) - FDA Registration e245e07e04f256e0ff40272f587f9851

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 e245e07e04f256e0ff40272f587f9851 and manufactured by Shijiazhuang Hipro Biotechnology Co.,ltd. The device was registered on October 20, 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.