Human Choionic Gonadotopin Test Kit (Immune Fluorescence Detection Method) - FDA Registration dc49054eff4fead6f8a28fdd779d3cda

Access comprehensive regulatory information for Human Choionic Gonadotopin Test Kit (Immune Fluorescence Detection Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID dc49054eff4fead6f8a28fdd779d3cda and manufactured by Shijiazhuang Hipro Biotechnology Co.,Ltd. The device was registered on December 20, 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.