WaveLight Oculyzer II System Diagnostic Device - FDA Registration CMDR-2025-03787

Access comprehensive regulatory information for WaveLight Oculyzer II System Diagnostic Device in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03787 and manufactured by Alcon Laboratories, Inc. in USA. The device was registered on January 31, 2025.

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