Philippines FDA registration CMDR-2025-04988

Philips DuraDiagnost Stationary Digital Radiographic System

Philippines·Philips Healthcare (Suzhou) Co., Ltd.- No. 258, ZhongYuan Road Suzhou Industrial Park 215024 Suzhou, Jiangsu Province People's Republic of China·China·Issued July 10, 2025 – July 10, 2030

Device information

Product Name: Philips DuraDiagnost Stationary Digital Radiographic System
Registration Number: CMDR-2025-04988

Manufacturer details

Manufacturer: Philips Healthcare (Suzhou) Co., Ltd.- No. 258, ZhongYuan Road Suzhou Industrial Park 215024 Suzhou, Jiangsu Province People's Republic of China
Country of Origin: China

Importer & distribution

Importer/Distributor: Philips Philippines, Inc.

Registration dates

Issuance Date: July 10, 2025
Expiry Date: July 10, 2030

About this record

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.