Terumo Ultimaster Nagomi Sirolimus Eluting Coronary Stent System - FDA Registration CMDR-2024-03357

Access comprehensive regulatory information for Terumo Ultimaster Nagomi Sirolimus Eluting Coronary Stent System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-03357 and manufactured by Terumo Europe N.V. - Interleuven 40 3001 Leuven Belgium Mfd. By: Terumo Corporation Ashitaka Plant - 150, Maimaigi-cho Fujinomiya-shi Shizuoka, 418- 0015 Japan in Japan. 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.