VENOFIX® SAFETY WINGED IV NEEDLE - FDA Registration MDR-01601

Access comprehensive regulatory information for VENOFIX® SAFETY WINGED IV NEEDLE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01601 and manufactured by B. Braun Melsungen AG in Malaysia. The device was registered on November 18, 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.