Edan Pulse Oximeter - FDA Registration CMDR-2025-04828

Access comprehensive regulatory information for Edan Pulse Oximeter in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04828 and manufactured by Edan Instruments, Inc. - #15 Jinhui ROad, Jinsha Community, Kengzi Sub-District, Pingshan DIstrict, 518122 Shenzhen, China in China. The device was registered on June 05, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Biosite Medical Instruments), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.