Technolas TENEO 317 Model 2 Laser System - FDA Registration CMDR-2024-02191

Access comprehensive regulatory information for Technolas TENEO 317 Model 2 Laser System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02191 and manufactured by Technolas Perfect Vision GmbH Messerschmittstr. 1+3, 80992 Munchen, Germany in Germany. The device was registered on January 03, 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.