POLYMED DOUBLE BLOOD BAG SYSTEM WITH CPDA - FDA Registration MDR-10375B

Access comprehensive regulatory information for POLYMED DOUBLE BLOOD BAG SYSTEM WITH CPDA in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10375B and manufactured by Poly Medicure Limited in India. The device was registered on September 22, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Iraseth Pharma 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.