POWERLINE™ PTCA CATHETER - FDA Registration MDR-06592

Access comprehensive regulatory information for POWERLINE™ PTCA CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06592 and manufactured by Biosensors Interventional Technologies Pte. Ltd. in Singapore. The device was registered on October 03, 2019.

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