CANACK 3-WAY SILICONE FOLEY CATHETER - FDA Registration MDR-10114B

Access comprehensive regulatory information for CANACK 3-WAY SILICONE FOLEY CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10114B and manufactured by Ningbo Luke Medical Devices Co., Ltd. in China. The device was registered on July 30, 2020.

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