FMS® FLUID MANAGEMENT SYSTEM INTERMEDIARY TUBING WITH ONE-WAY VALVE - FDA Registration MDR-09819

Access comprehensive regulatory information for FMS® FLUID MANAGEMENT SYSTEM INTERMEDIARY TUBING WITH ONE-WAY VALVE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09819 and manufactured by Harmac Medical Products, Inc. - Nueva, Tijuana CP Mexico mfd. By: Depuy Mitek, Inc. - MA, USA in USA. The device was registered on October 21, 2021.

This page provides complete registration details including manufacturer information, importer/distributor details (Johnson & Johnson (Phils), 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.