Creatinine Assay Kit (PAP) - FDA Registration 8beb61b0980287ce8df835b56c8e9270

Access comprehensive regulatory information for Creatinine Assay Kit (PAP) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8beb61b0980287ce8df835b56c8e9270 and manufactured by Shenzhen New Industries Biomedical Engineering Co., Ltd.,. The device was registered on March 28, 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.