Hemosep® Cell Concentrator Pack - FDA Registration CMDR-2025-05142

Access comprehensive regulatory information for Hemosep® Cell Concentrator Pack in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-05142 and manufactured by Brightwake Limited - Lowmoor Business Park, Kirkby in Ashfield, Nottinghamshire, NG17 7JZ, United Kingdom in United Kingdom. The device was registered on July 09, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Dubbel Medical Corporation), 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.