Carcinoembryonic antigen Test Kit (NephelometryimmunoassayMethod). - FDA Registration 265a9e2bce68ccf2fe3b7df6a0a45157

Access comprehensive regulatory information for Carcinoembryonic antigen Test Kit (NephelometryimmunoassayMethod). in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 265a9e2bce68ccf2fe3b7df6a0a45157 and manufactured by ShijiazhuangHiproBiotechnologyCo.,ltd. The device was registered on August 23, 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.