BRK™ TRANSSEPTAL NEEDLE - FDA Registration MDR-02928A

Access comprehensive regulatory information for BRK™ TRANSSEPTAL NEEDLE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-02928A and manufactured by Abbott Vascular (Singapore) Pte. Ltd. - Singapore mfd. By: St. Jude Medical - 14901 DeVeau Place Minnetonka, MN, USA in USA. The device was registered on September 28, 2021.

This page provides complete registration details including manufacturer information, importer/distributor details (Biodevices, 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.