Surgitech Butterfly Needle without Luer Adapter Blood Collection Needle - FDA Registration CMDR-2025-05139

Access comprehensive regulatory information for Surgitech Butterfly Needle without Luer Adapter Blood Collection Needle in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-05139 and manufactured by Liuyang Sanli Medical Technology Development Co., Ltd. - No.99, Jinsha North Road 410300 Liuyang, Hunan People's Republic of China in China. The device was registered on July 14, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Medasia Medical Products 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.