GelPOINT® Path Transanal Access Platform - FDA Registration CMDR-2025-04102

Access comprehensive regulatory information for GelPOINT® Path Transanal Access Platform in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04102 and manufactured by Applied Medical Resources Corporation - 22872 Avenida Empresa Rancho Santa Margarita, California 92688, United States Mfd. By: Applied Medical Resources Corporation - 29977 Avenida de las Banderas, Rancho Santa Margarita, California 92688, United States in USA. The device was registered on March 12, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (RBGM Medical Express Sales, 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.