Bausch + Lomb Bipolar Eraser, Lemo Tapered - FDA Registration CMDR-2024-02393

Access comprehensive regulatory information for Bausch + Lomb Bipolar Eraser, Lemo Tapered in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02393 and manufactured by Bausch & Lomb GmbH Im Schuhmachergewann 4, 69123 Heidelberg, Germany in Germany. The device was registered on March 04, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Bausch & Lomb 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.