DR. KELLY NEBULIZER KIT WITH AEROSOL MASK - FDA Registration MDR-09659

Access comprehensive regulatory information for DR. KELLY NEBULIZER KIT WITH AEROSOL MASK in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09659 and manufactured by Ningbo Foyomed Medical Instruments Co., Ltd. in China. The device was registered on May 13, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Medical Center Trading 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.