PROXIMATE® PROCEDURE FOR PROLAPSE AND HEMORRHOIDS (PPH) SET - FDA Registration DVR-4595
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-4595 and manufactured by Ethicon Endo-Surgery, LLC in Mexico. The device was registered on September 06, 2019.
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.

