Renaux Hemodialysis Catheter Kit - Triple Lumen - FDA Registration CMDR-2025-05032B

Access comprehensive regulatory information for Renaux Hemodialysis Catheter Kit - Triple Lumen in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-05032B and manufactured by Guangdong Baihe Medical Technology Co., Ltd. - No. 89, Taoyuan East Road, Nanhai, Foshan, Guangdong Province, P.R.China in China. The device was registered on July 11, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Josmef Enterprises), 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.