EDAN Patient Monitor - FDA Registration CMDR-2025-04971A

Access comprehensive regulatory information for EDAN Patient Monitor in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04971A and manufactured by EDAN Instruments, Inc. - 15 Jinhui Rd., Jinsha Community, Kengzi Subdistrict, Pingshan District, Shenzhen, 518122 P.R.China in China. The device was registered on July 10, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Sunfu Solutions, Inc.), 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.