Proximate™ Plus MD Multi-Directional Skin Stapler - FDA Registration DVR-6930

Access comprehensive regulatory information for Proximate™ Plus MD Multi-Directional Skin Stapler in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-6930 and manufactured by Ethicon Endo-Surgery, LLC Guaynabo, Puerto Rico, USA Mfd By: Nypro Healthcare Baja Inc. - Chihuahua, Mexico in USA. The device was registered on May 30, 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.