Optio A.V. Fistula Needle, Single Use - FDA Registration CMDR-2025-04689

Access comprehensive regulatory information for Optio A.V. Fistula Needle, Single Use in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04689 and manufactured by Jiangxi Hongda Medical Equipment Group Ltd. - 39 South Shenglu Rd., Jinxian Country 331700 Nanchang, Jiangi Province, People's Republic of China in China. The device was registered on June 16, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Infilife Corporation), 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.