Terufusion® Blood Administration Set for Infusion Pump - FDA Registration MDR-01403

Access comprehensive regulatory information for Terufusion® Blood Administration Set for Infusion Pump in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01403 and manufactured by Terumo Medical Products (Hangzhou) Co., Ltd. - M4-9-5 Hangzhou Economic & Technological Development Zone 310018 Hangzhou, People's Republic of China in China. 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.