Biner LC Light Curing Type Cavity Liner - FDA Registration MDR-04850

Access comprehensive regulatory information for Biner LC Light Curing Type Cavity Liner in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04850 and manufactured by Meta Biomed Co., Ltd. 270 Osongsaengmyeong 1-ro, Osong-eup, Heungdeok-gu, Cheongju-si, Chungcheongbuk-do, Korea in Korea. The device was registered on October 07, 2022.

This page provides complete registration details including manufacturer information, importer/distributor details (Value-Rx, 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.