APC-60i PRP PROCEDURE PACK; Size/Code: 51407 - FDA Registration MDR-08792F

Access comprehensive regulatory information for APC-60i PRP PROCEDURE PACK; Size/Code: 51407 in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08792F and manufactured by Terumo BCT, Inc. - Lakewood, CO, USA in USA. The device was registered on June 10, 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.