C-reactive Test Kit (Rate Scattering Turbidimetric Method) - FDA Registration a858aa69d8078d5f7d5c8a719142f0eb

Access comprehensive regulatory information for C-reactive 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 a858aa69d8078d5f7d5c8a719142f0eb and manufactured by Shijiazhuang Hipro Biotechnology Co.,Ltd. The device was registered on February 01, 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.