SV .018’’ STEERABLE GUIDEWIRES - FDA Registration MDR-01551

Access comprehensive regulatory information for SV .018’’ STEERABLE GUIDEWIRES in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01551 and manufactured by Cordis Corporation- 14201 North West 60th Avenue, Miami Lakes, Florida, 33014, USA Mfd by: Lake Region Medical Ltd.- Butlersland New Ross Co. Wexford Ireland in Ireland. The device was registered on March 05, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Getz Bros. 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.