TWINFIX ULTRA HA WITH NEEDLE - FDA Registration MDR-09929

Access comprehensive regulatory information for TWINFIX ULTRA HA WITH NEEDLE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09929 and manufactured by Smith & Nephew Endoscopy in USA. The device was registered on July 08, 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.