OKTA-LINE PERFLUORO-OCTANE LIQUID - FDA Registration DVR-6187

Access comprehensive regulatory information for OKTA-LINE PERFLUORO-OCTANE LIQUID in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-6187 and manufactured by Bausch & Lomb, Inc. in Ireland. The device was registered on April 29, 2019.

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.