SIMPLEX® FOLEY CATHETER - FDA Registration MDR-07557

Access comprehensive regulatory information for SIMPLEX® FOLEY CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07557 and manufactured by Well Lead Medical Co., Ltd. in China. The device was registered on November 05, 2019.

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