Mindray Syringe Pump BeneFusion eSP - FDA Registration CMDR-2025-04903A

Access comprehensive regulatory information for Mindray Syringe Pump BeneFusion eSP in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04903A and manufactured by Shenzhen Mindray Scientific Co., Ltd. - 6/F, Bldg. 2, 1203 Nanhuan Avenue, Yutang Block, Guangming District, 518106 Shenzhen, People's Republic of China in China. The device was registered on June 26, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Mindray Medical International Philippines, 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.