CORTEX SCREW (SELF-TAPPING) - FDA Registration MDR-08212

Access comprehensive regulatory information for CORTEX SCREW (SELF-TAPPING) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08212 and manufactured by Synthes GmbH in Switzerland. The device was registered on April 29, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Johnson & Johnson (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.