PROXIMATE® Procedure for Prolapse and Hemorrhoids (PPH) Set - FDA Registration DVR-4945

Access comprehensive regulatory information for PROXIMATE® Procedure for Prolapse and Hemorrhoids (PPH) Set in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-4945 and manufactured by Ethicon Endo-Surgery, LLC 475 Calle C, Guaynabo, Puerto Rico 00969, USA Mfd By: Nypro Healthcare Baja Inc. - Avenida de las Torres 7125, Colonia Salvarcar 118, Ciudad Juarez, Chihuahua 32580, Mexico in USA. The device was registered on December 18, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Johnson & Johnson (Phils.), 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.