Spectra Optia Apheresis System - FDA Registration CMDR-2025-04121

Access comprehensive regulatory information for Spectra Optia Apheresis System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04121 and manufactured by Terumo BCT, Inc. - 10811 W. Collins Ave., Lakewood, Colorado 80215 USA in USA. The device was registered on March 12, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Terumo Marketing 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.