WILTROM INTERBODY FUSION SYSTEM - FDA Registration MDR-10949

Access comprehensive regulatory information for WILTROM INTERBODY FUSION SYSTEM in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10949 and manufactured by Wiltrom Co. Ltd. - Hsinchu County, Taiwan, R.O.C. in China. The device was registered on July 08, 2021.

This page provides complete registration details including manufacturer information, importer/distributor details (Mular Medical Distribution, 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.