Compoflex 3F 63mL CPDA-1-PDS-V BLOOD BAG - FDA Registration MDR-06423D

Access comprehensive regulatory information for Compoflex 3F 63mL CPDA-1-PDS-V BLOOD BAG in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06423D and manufactured by Fresenius Kabi Asia Pacific Ltd. in Germany. The device was registered on May 17, 2019.

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.