Diapact® CRRT Plasma Absorption Perfusion Kit - FDA Registration MDR-05943

Access comprehensive regulatory information for Diapact® CRRT Plasma Absorption Perfusion Kit in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05943 and manufactured by B. Braun Avitum AG Schwarzenberger Weg 73-39, 34212 Melsungen Germany Mfd By: B. Braun Avitum Italy S.p.A - Via XXV Luglio 11, 41037 Mirandola (MO), Italy in Germany. The device was registered on January 09, 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.