Philippines FDA registration CMDR-2025-04339

WallFlex™ Duodenal Soft Stent System with Anchor Lock Delivery System

Philippines flagPhilippines·Boston Scientific Corporation 300 Boston Scientific Way Marlborough MA 01752 USA Mfd By: Boston Scientific Limited - Ballybrit Business Park Galway, Ireland·USA·Issued May 06, 2025 – May 06, 2030
Device information
Product Name
WallFlex™ Duodenal Soft Stent System with Anchor Lock Delivery System
Registration Number
CMDR-2025-04339
Manufacturer details
Country of Origin
USA
Importer & distribution
Registration dates
Issuance Date
May 06, 2025
Expiry Date
May 06, 2030
About this record

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.

Free DatabasePowered by Pure Global AIFDA Official DataUSA