Access comprehensive regulatory information for in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07546 and manufactured by in . The device was registered on May 13, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Bone Fix Metal Craft 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.