Diacap® Pro - FDA Registration MDR-05072

Access comprehensive regulatory information for Diacap® Pro in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05072 and manufactured by B. Braun Avitum AG Schwarzenberher Weg 73-79, 34212 Melsungen, Germany Mfd. By: B. Braun Avitum Saxonia GmbH - Juri Gagarin-Strasse 13, 01454 Redeberg, Germany in Germany. The device was registered on January 31, 2023.

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