Low Density Lipoprotein Cholesterol Test Kit (Enzymic Method) - FDA Registration 9a34b95aad0089cc54808b9d46ac5868

Access comprehensive regulatory information for Low Density Lipoprotein Cholesterol Test Kit (Enzymic Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9a34b95aad0089cc54808b9d46ac5868 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.