SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR - FDA Registration MDR-09906

Access comprehensive regulatory information for SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09906 and manufactured by Smith & Nephew Pte. Ltd. in USA. The device was registered on July 02, 2020.

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