Bausch & Lomb Laser Ptobe Standard - FDA Registration MDR-0486701

Access comprehensive regulatory information for Bausch & Lomb Laser Ptobe Standard in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-0486701 and manufactured by Peregrine Surgical Ltd. 51 Britain Drive, New Britain, PA 18901, USA in USA. The device was registered on January 15, 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.