Braster Pro Breast Examination System - FDA Registration CMDR-2024-02790

Access comprehensive regulatory information for Braster Pro Breast Examination System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02790 and manufactured by Braster Spolka Akcyjna (Braster S.A.) Cichy Ogrod 7, Szeligi, 05-850 Ozarow, Mazowiecki, Poland in Poland. The device was registered on May 07, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Mular Medical Distribution 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.