Diacap® Pro High Flux Dialyzer - FDA Registration MDR-05072B

Access comprehensive regulatory information for Diacap® Pro High Flux Dialyzer in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05072B and manufactured by B. Braun Avitum AG Schwerzenberher Weg 73-79, 34212 Melsungen, Germany Mfd By: B. Braun Avitum Saxonia GmbH - Juri Gagarin-Strasse 13, 01454 Radeberg, Germany in Germany. The device was registered on March 26, 2024.

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.