INFUSOMAT SPACE LINE INFUSION PUMP ADMINISTRATION SET - FDA Registration MDR-01835

Access comprehensive regulatory information for INFUSOMAT SPACE LINE INFUSION PUMP ADMINISTRATION SET in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01835 and manufactured by B. Braun Melsungen AG in Malaysia. The device was registered on April 01, 2020.

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.