HI-TORQUE (HT) VERSATURN, ULTRAFLEX GUIDE WIRE, STRAIGHT TIP - FDA Registration MDR-05917A

Access comprehensive regulatory information for HI-TORQUE (HT) VERSATURN, ULTRAFLEX GUIDE WIRE, STRAIGHT TIP in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05917A and manufactured by Abbott Vascular Netherlands B.V. in The Netherlands. The device was registered on October 23, 2018.

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.