SIMPLEX® Foley Catheter, 2-Way, with - FDA Registration MDR-05022 B

Access comprehensive regulatory information for SIMPLEX® Foley Catheter, 2-Way, with in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05022 B and manufactured by Fuzhou Kanglite Medical Apparatus Co., Ltd. - Room 02, No. 17 Floor West Jinyuan Plaza, No. 68, Guangda Road, Taijang, Fuzhou, 350005, Fujian, P.R. China in China. The device was registered on July 21, 2023.

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.