UNIMEX NELATON CATHETER - FDA Registration MDR-05773

Access comprehensive regulatory information for UNIMEX NELATON CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05773 and manufactured by Ningbo Greatcare Trading Co., Ltd. in China. The device was registered on August 29, 2018.

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