Intraplas Duodenal Tube - FDA Registration MDR-06921

Access comprehensive regulatory information for Intraplas Duodenal Tube in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06921 and manufactured by Kenxin International Company Ltd. Room 714, West Tower No. 140 West Zhongshan Avenue, Tianhe District, Huagang Office Building, Guangzhou City, Guangdong Province, China in China. The device was registered on June 04, 2024.

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