RESPISENZ OXYGEN CANNULA - FDA Registration MDR-07931

Access comprehensive regulatory information for RESPISENZ OXYGEN CANNULA in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07931 and manufactured by Ningbo Greatcare Trading Co., Ltd. in China. The device was registered on August 05, 2020.

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.