Cutter - FDA Registration fe8cc49fd7c190b67bac7b4ea421df70

Access comprehensive regulatory information for Cutter in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID fe8cc49fd7c190b67bac7b4ea421df70 and manufactured by Jeil Medical Corporation. The device was registered on December 29, 2021.

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.