Terumo Terufusion® Administration Set E - FDA Registration DVR-8860

Access comprehensive regulatory information for Terumo Terufusion® Administration Set E in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-8860 and manufactured by Terumo Corporation - 44-1, 2-chome, Hatagaya, Shibuya-ku, Tokyo 151-0072 Japan in Japan. The device was registered on August 06, 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.