Bausch + Lomb Laser Probe Standard Curved - FDA Registration MDR-06314

Access comprehensive regulatory information for Bausch + Lomb Laser Probe Standard Curved in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06314 and manufactured by Penegrine Surgical Ltd. 51 Britain Drive, New Britain, PA 18901 USA in USA. The device was registered on January 09, 2024.

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