SIMPLEX® DUODENAL TUBE, NGT/LEVIN - FDA Registration MDR-01624

Access comprehensive regulatory information for SIMPLEX® DUODENAL TUBE, NGT/LEVIN in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01624 and manufactured by Ningbo Greatcare Trading Co., Ltd. Unit 93, Building 12, No. 818, Qiming Road, Yinzhou, 315105 Ningbo, Zhejiang, China Mfd By: Well Lead Medical Co., Ltd. - No. 47 Guomao Avenue Zouth, 511434 Panyu, Guangzhou, People's Republic of China in China. The device was registered on December 19, 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.