ABX Pentra Precitest Solution - FDA Registration f017bfbc4cd10b763a1a9867db0b8dfe

Access comprehensive regulatory information for ABX Pentra Precitest Solution in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f017bfbc4cd10b763a1a9867db0b8dfe and manufactured by HORIBA ABX SAS. The device was registered on January 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.