ABX Basolyse 5L - FDA Registration 3b82c0758975cc25cd4370aa73f7fb24

Access comprehensive regulatory information for ABX Basolyse 5L in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3b82c0758975cc25cd4370aa73f7fb24 and manufactured by HORIBA ABX SAS. The device was registered on January 27, 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.