ARTHREX® BONE CUTTER - FDA Registration MDR-08117A

Access comprehensive regulatory information for ARTHREX® BONE CUTTER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08117A and manufactured by Arthrex, Inc. - 1370 Creekside Blvd., Naples Florida, USA in USA. The device was registered on July 10, 2025.

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