Pulse Oximeter - FDA Registration 82e3443f4d553b0c8a0bf1d2fc4f3a75

Access comprehensive regulatory information for Pulse Oximeter in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 82e3443f4d553b0c8a0bf1d2fc4f3a75 and manufactured by Shenzhen Aeon Technology Co., Ltd. The device was registered on June 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.