FIGHTER™ GUIDEWIRE - FDA Registration MDR-07876

Access comprehensive regulatory information for FIGHTER™ GUIDEWIRE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07876 and manufactured by Boston Scientific Corporation in Japan. The device was registered on April 01, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Boston Scientific Phils., 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.