BIOSURE GUIDEWIRE - FDA Registration MDR-10543

Access comprehensive regulatory information for BIOSURE GUIDEWIRE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10543 and manufactured by Smith & Nephew Pte. Ltd. - Singapore mfd. By: AthroCare Corporation - Alajuela, Costa Rica For: Smith & Nephew Inc., Endoscopy Division - Andover, MA, USA in USA. The device was registered on October 29, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Endomed Trading, 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.