PhoenixSpec™ Nephelometer and Calibrator Kits - FDA Registration 1021228494bf64c77f0dbd084e182c56

Access comprehensive regulatory information for PhoenixSpec™ Nephelometer and Calibrator Kits in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 1021228494bf64c77f0dbd084e182c56 and manufactured by Becton, Dickinson and Company. The device was registered on October 06, 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.