MODUS MEDARTIS 1.5 CMF SYSTEM SET, 1.5 CORTICAL SCREWS, SELF-DRILLING CROSS-DRIVE - FDA Registration MDR-08949D

Access comprehensive regulatory information for MODUS MEDARTIS 1.5 CMF SYSTEM SET, 1.5 CORTICAL SCREWS, SELF-DRILLING CROSS-DRIVE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08949D and manufactured by Medartis AG in Switzerland. The device was registered on November 22, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (Dubbel Medical Corporation), 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.