Simplex® Endotracheal Tube Cuffed (Sterile) - FDA Registration DVR-5774

Access comprehensive regulatory information for Simplex® Endotracheal Tube Cuffed (Sterile) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-5774 and manufactured by Ningbo Greatcare Trading Co. Ltd.- Unit 93, Building 12, No. 818, Qiming Road, Yinzhou, Ningbo 315105, Zheijang, China Mfd by: Well Lead Medical Co. Ltd.- C-4 Jinhu Industrial Estate, Hualong 511434 Panyu, Guangzhou, China in China. The device was registered on October 10, 2024.

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