PTFE ANGIOGRAPHIC GUIDEWIRE - FDA Registration MDR-09977

Access comprehensive regulatory information for PTFE ANGIOGRAPHIC GUIDEWIRE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09977 and manufactured by Medtronic International Ltd. in USA. The device was registered on July 08, 2020.

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