Reagent - FDA Registration dc8f80b88af961c880e677525471f8d1

Access comprehensive regulatory information for Reagent in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID dc8f80b88af961c880e677525471f8d1 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The device was registered on December 15, 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.