CELSITE® ARTERIAL ACCESS PORT FOR ARTERIAL ACCESS - FDA Registration MDR-06599A

Access comprehensive regulatory information for CELSITE® ARTERIAL ACCESS PORT FOR ARTERIAL ACCESS in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06599A and manufactured by B. Braun Medical in France. The device was registered on April 29, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (B. Braun Medical Supplies, 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.