BD Nexiva™ Clsoed IV Catheter System-Dual Port - FDA Registration CMDR-2025-04384

Access comprehensive regulatory information for BD Nexiva™ Clsoed IV Catheter System-Dual Port in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04384 and manufactured by Becton Dickinson Holdings Pte Ltd. 2 International Buisness Park Road, The Strategy #08-08, Singapore 609930 Mfd By: Becton Dickinson Infusion Therapy Sysyems Inc. - 9450 South State Sandy, Utah 84070 USA in Singapore. The device was registered on May 06, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Getz Bros. 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.