TERUMO RADIFOCUS OPTITORQUE ANGIOGRAPHIC CATHETER - FDA Registration DVR-5037

Access comprehensive regulatory information for TERUMO RADIFOCUS OPTITORQUE ANGIOGRAPHIC CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-5037 and manufactured by Terumo Corporation in Japan. The device was registered on August 13, 2020.

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.