Pentra XLR - FDA Registration e46952e35eac99444a9d1d8d536659a0

Access comprehensive regulatory information for Pentra XLR in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e46952e35eac99444a9d1d8d536659a0 and manufactured by HORIBA ABX SAS. The device was registered on September 07, 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.