Leforte System ( Bone Plate ) - FDA Registration 8b67554701ede7568b1d3383763b122d

Access comprehensive regulatory information for Leforte System ( Bone Plate ) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8b67554701ede7568b1d3383763b122d and manufactured by Jeil Medical Corporation. The device was registered on August 02, 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.