Endopath® Xcel™ Dilating Tip Trocar with Stability Sleeve - FDA Registration CMDR-2025-04739

Access comprehensive regulatory information for Endopath® Xcel™ Dilating Tip Trocar with Stability Sleeve in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04739 and manufactured by Ethicon Endo-Surgery, LLC - 475 Calle C, Guaynabo, Puerto Rico 00969 USA Mfd. By: Nypro Precision Assembles (NPA) de Mexico S. De R.L. De C.V. - Blvd. Hector Teran Teran #20662-C, Col. Murua Oriente, Tijuana, 22465, Mexico in USA. The device was registered on July 10, 2025.

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