PRONTOSAN® WOUND SOLUTION - FDA Registration MDR-06523B

Access comprehensive regulatory information for PRONTOSAN® WOUND SOLUTION in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06523B and manufactured by B. Braun Medical AG in Germany. The device was registered on January 23, 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.