PRIMERA + ENDOTRACHEAL TUBE - FDA Registration MDR-07783A

Access comprehensive regulatory information for PRIMERA + ENDOTRACHEAL TUBE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07783A and manufactured by Jiangxi Hongda Medical Equipment Group Ltd. in China. The device was registered on July 10, 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.