DIASTREAM A/V BLOODLINES FOR HAEMODIALYSIS BLOOD TUBING SET - FDA Registration MDR-072302I

Access comprehensive regulatory information for DIASTREAM A/V BLOODLINES FOR HAEMODIALYSIS BLOOD TUBING SET in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-072302I and manufactured by B. Braun Avitum AG in Vietnam. The device was registered on November 25, 2019.

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.