Bausch+ Lomb Stellaris Elite Vision Enhancement System - FDA Registration CMDR-2023-02625

Access comprehensive regulatory information for Bausch+ Lomb Stellaris Elite Vision Enhancement System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2023-02625 and manufactured by Bausch and Lomb Incorporated 1400 North Goodman Street, Rochester, NY 14609 USA Mfd By: Bausch and Lomb Incorporated - 3365 Tree Court Industrial Boulevard, St. Louis, MO 63122 USA in USA. The device was registered on April 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.