ENDOPATH® ELECTROSURGERY PROBE PLUS II - FDA Registration DVR-4982

Access comprehensive regulatory information for ENDOPATH® ELECTROSURGERY PROBE PLUS II in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-4982 and manufactured by Ethicon Endo-Surgery, LLC in Mexico. The device was registered on October 09, 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.