Single Use Ligating Device - FDA Registration 5c02622a06fc8b4bebc7bc75f6365e28

Access comprehensive regulatory information for Single Use Ligating Device in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5c02622a06fc8b4bebc7bc75f6365e28 and manufactured by Aomori Olympus 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.