Haemoselect® L. 07 Plasma Filter - FDA Registration MDR-06598B

Access comprehensive regulatory information for Haemoselect® L. 07 Plasma Filter in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06598B and manufactured by B. Braun Avitum AG Schwarzenberg Weg 73-79 34212 Melsungen Germany Mfd By: B. Braun Avitum Italy S.p.A - Via XXV Luglio 11 41037 Mirandola, Italy in Germany. The device was registered on May 22, 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.