BeneVision N19 - FDA Registration CMDR-2025-04319

Access comprehensive regulatory information for BeneVision N19 in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04319 and manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd. in China. The device was registered on April 22, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Respicare Enterprises, Incorporated), 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.