PRIMERA + 2-WAY LATEX FOLET CATHETER - FDA Registration MDR-07235

Access comprehensive regulatory information for PRIMERA + 2-WAY LATEX FOLET CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07235 and manufactured by Ningbo Greetmed Medical Instruments Co., Ltd. in China. The device was registered on May 28, 2020.

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