UROMAX ULTRA™ BALLOON DILATATION CATHETER - FDA Registration MDR-01843

Access comprehensive regulatory information for UROMAX ULTRA™ BALLOON DILATATION CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01843 and manufactured by Boston Scientific Corporation in Ireland. The device was registered on March 18, 2020.

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