Philips Lumify Diagnostic Ultrasound System - FDA Registration CMDR-2025-04924

Access comprehensive regulatory information for Philips Lumify Diagnostic Ultrasound System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04924 and manufactured by Philips Ultrasound LLC- 22100 Bothell Everett Highway, Bothell, WA 98021 USA in USA. 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.