Reveos - FDA Registration CMDR-2024-03383

Access comprehensive regulatory information for Reveos in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-03383 and manufactured by Terumo BCT, Inc. - 10811 W. Collins Ave., Lakewood, Colorado 80215 USA in USA. The device was registered on October 30, 2024.

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.