Philips Xper Information Management System - FDA Registration CMDR-2025-04922

Access comprehensive regulatory information for Philips Xper Information Management System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04922 and manufactured by Philips Medical Systems Nederland B.V.- Veenpluis 6 5684 PC Best The Netherlands Mfd. By: Philips Clinical Informatics- Sistema de Informaҫão Ltda Rua Dois de Setembro 1944 89052-004 Blumenau, SC Brazil in The Netherlands. The device was registered on June 26, 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.