MANI K-FILES - FDA Registration 16f9674ae6bd6583da27be99069a1104

Access comprehensive regulatory information for MANI K-FILES in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 16f9674ae6bd6583da27be99069a1104 and manufactured by MANI HANOI CO., LTD. The device was registered on March 22, 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.