Dosi-Flow 30 MP SESE I.V. Flow Regulator with Infusion Set - FDA Registration MDR-01035

Access comprehensive regulatory information for Dosi-Flow 30 MP SESE I.V. Flow Regulator with Infusion Set in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01035 and manufactured by Leventon, S.A.U - Ronda Can Margarit 38 Pol. Ind. Can Margarit 08635 Sant Esteve Sesrovires, Barcelona, Spain in Spain. The device was registered on June 13, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (South East Star Enterprises), 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.