BD VENFLON™ PRO SAFETY / BD INSTAFLASH™ NEEDLE TECHNOLOGY NEEDLE PROTECTED IV CANNULA (E-BEAM STERILIZED) - FDA Registration CMDR-2021-00117

Access comprehensive regulatory information for BD VENFLON™ PRO SAFETY / BD INSTAFLASH™ NEEDLE TECHNOLOGY NEEDLE PROTECTED IV CANNULA (E-BEAM STERILIZED) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2021-00117 and manufactured by Becton Dickinson Infusion Therapy AB - Helsingborg, Sweden mfd. By: BD Medical (S) Pte. Ltd. - Tuas Avenue 2, Singapore in Singapore. The device was registered on July 02, 2021.

This page provides complete registration details including manufacturer information, importer/distributor details (KSM Healthcare, 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.