BARD INLAY VERSAFIT MULTILENGTH URETERAL STENT WITHOUT GUIDEWIRE - FDA Registration DVR-6407

Access comprehensive regulatory information for BARD INLAY VERSAFIT MULTILENGTH URETERAL STENT WITHOUT GUIDEWIRE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-6407 and manufactured by Bard Shannon Ltd. in USA. The device was registered on October 03, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (Healthsolutions Enterprises 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.