ARTHREX® SYNDESMOSIS TIGHTROPE® XP IMPLANT, STAINLESS STEEL - FDA Registration MDR-10049E

Access comprehensive regulatory information for ARTHREX® SYNDESMOSIS TIGHTROPE® XP IMPLANT, STAINLESS STEEL in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10049E and manufactured by Arthrex, Inc. in USA. The device was registered on July 23, 2020.

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.