VEDKANG HYDROPHILIC GUIDE WIRE - FDA Registration MDR-09514A

Access comprehensive regulatory information for VEDKANG HYDROPHILIC GUIDE WIRE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09514A and manufactured by Jiangsu Vedkang Medical Science & Technology Co., Ltd. - Jiangsu, China in China. The device was registered on October 27, 2021.

This page provides complete registration details including manufacturer information, importer/distributor details (Alfamed Care Enterprise), 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.