ECHELON™ 3000 Stapler - FDA Registration CMDR-2025-04653B

Access comprehensive regulatory information for ECHELON™ 3000 Stapler in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04653B 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, 32580 Ciudad Juarez, Chihuahua, Mexico in USA. The device was registered on May 14, 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.