Tappa Endotracheal Tube (PVC Reinforced) - FDA Registration CMDR-2024-02950

Access comprehensive regulatory information for Tappa Endotracheal Tube (PVC Reinforced) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02950 and manufactured by Hangzhou Tappa Medical Technology Co., Ltd. No. 225 Chutian Rd., binjiang District 310000 Hangzhou, China in China. The device was registered on June 05, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (RMG Hospital Supply, 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.