MARKSMAN ™ CATHETER SINGLE LUMEN CATHETER - FDA Registration MDR-07645

Access comprehensive regulatory information for MARKSMAN ™ CATHETER SINGLE LUMEN CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07645 and manufactured by Medtronic International Limited 49 Changi South Avenue 2 Singapore mfd. by: Medtronic Mexico S. de R.L. de CV - Av. Paseo Cucapah, 10510 El Lago, C.P. 22210 Tijuana Baja California, Mexico For Micro Therapeutics, Inc. - d/b/a ev3 Neurovascular 9775 Toledo Way lrvine, CA 92618 USA in USA. The device was registered on February 19, 2025.

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.