WallFlex™ Duodenal Soft Stent System with Anchor Lock Delivery System - FDA Registration CMDR-2025-04339

Access comprehensive regulatory information for WallFlex™ Duodenal Soft Stent System with Anchor Lock Delivery System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04339 and manufactured by Boston Scientific Corporation 300 Boston Scientific Way Marlborough MA 01752 USA Mfd By: Boston Scientific Limited - Ballybrit Business Park Galway, Ireland in USA. The device was registered on May 06, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Boston Scientific Philippines, 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.