BMAC2-120n BONE MARROW PROCEDURE PACK - FDA Registration MDR-08796I

Access comprehensive regulatory information for BMAC2-120n BONE MARROW PROCEDURE PACK in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08796I and manufactured by Terumo BCT, Inc. - Lakewood, CO, USA in USA. The device was registered on June 11, 2021.

This page provides complete registration details including manufacturer information, importer/distributor details (Terumo Markerting 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.