TRO-UROCATH Foley Balloon Catheter (3 way) - FDA Registration CMDR-2023-01313
Access comprehensive regulatory information for TRO-UROCATH Foley Balloon Catheter (3 way) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2023-01313 and manufactured by Troge Medical GmbH Milchstraฮฒe 19, 20148 Hamburg, Deutschland in Deutschland. The device was registered on February 14, 2024.
This page provides complete registration details including manufacturer information, importer/distributor details (Healthsolutions Enterprises 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.
