BD Alaris™ GP Volumetric Pump Alaris™ Safety Clamp SmartSite™ Needle-free Syste, - FDA Registration CMDR-2025-04105

Access comprehensive regulatory information for BD Alaris™ GP Volumetric Pump Alaris™ Safety Clamp SmartSite™ Needle-free Syste, in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04105 and manufactured by Becton Dickinson Holdings Pte. Ltd. - 2 International Business Park Road, The Strategy #08-08, Singapore 609930 Mfd. By: CareFusion BH 335 d.o.o. Cazin Mihaljevac bb Cazin 77220 Bosnia & Herzegovina For: BD Switzerland Sàrl - Route de Crassier 17, Business Park Terre-Bonne, Batiment A4, 1262 Eysins, Switzerland in Switzerland. The device was registered on March 12, 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.