Surgitech Scalp Vein Set - FDA Registration CMDR-2025-03783

Access comprehensive regulatory information for Surgitech Scalp Vein Set in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03783 and manufactured by Ningbo Greetmed Medical Instruments Co., Ltd. in China. The device was registered on January 31, 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.