Philips DuraDiagnost Stationary Digital Radiographic System - FDA Registration CMDR-2025-04988

Access comprehensive regulatory information for Philips DuraDiagnost Stationary Digital Radiographic System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04988 and manufactured by Philips Healthcare (Suzhou) Co., Ltd.- No. 258, ZhongYuan Road Suzhou Industrial Park 215024 Suzhou, Jiangsu Province People's Republic of China in China. The device was registered on July 10, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Philips 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.