Philips StentBoost Live - FDA Registration CMDR-2025-05127

Access comprehensive regulatory information for Philips StentBoost Live in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-05127 and manufactured by Philips Medical Systems Nederland B.V. - Veenpluis 6 5684 PC Best The Netherlands in The Netherlands. The device was registered on July 17, 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.