Endure Arteriovenous Fistula Needle - FDA Registration CMDR-2024-2658

Access comprehensive regulatory information for Endure Arteriovenous Fistula Needle in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-2658 and manufactured by Farmasol Tibbi Urunler San Ve Tic A.S. Organize Sanayi Bolgesi 18, Cad. No. 7 Melikgazi Kayseri Turkey in Turkey. The device was registered on April 17, 2024.

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