Bausch + Lomb Entry Site Alignment System with Valve - FDA Registration CMDR-2024-02842

Access comprehensive regulatory information for Bausch + Lomb Entry Site Alignment System with Valve in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02842 and manufactured by Bausch & Lomb Incorporated 1400 North Goodman St. Rochester, NY 14609, USA Mfd By: Roechling Medical Lancaster, LLC - 44 Denver Road, Denver, PA 17517, USA in USA. The device was registered on May 15, 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.