Apheresis System - FDA Registration CMDR-2025-04436

Access comprehensive regulatory information for Apheresis System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04436 and manufactured by Fresenius Kabi AG Fresenius Hemocare GmbH in Germany Germany. The device was registered on April 25, 2025.

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