SOFTSILK INTERFERENCE SCREW - FDA Registration MDR-10189

Access comprehensive regulatory information for SOFTSILK INTERFERENCE SCREW in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10189 and manufactured by Smith & Nephew Pte. Ltd. in USA. The device was registered on August 06, 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.