STARTER™ GUIDEWIRE - FDA Registration MDR-01991

Access comprehensive regulatory information for STARTER™ GUIDEWIRE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01991 and manufactured by Cardiac Pacemakers Inc. (Boston Scientific Corporation) - 4100 Hamline Avenue North, St. Paul, MN, 55112-5798, USA mfd. By: Boston Scientific Limited- Cashel Road Clonmel, Co. Tipperary Ireland in Ireland. The device was registered on April 22, 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.