MANI Reamers - FDA Registration 338c45e0c71a3fbf68a41f58e6c70d21

Access comprehensive regulatory information for MANI Reamers in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 338c45e0c71a3fbf68a41f58e6c70d21 and manufactured by MANI HANOI CO., LTD. The device was registered on April 01, 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.