REBORN ESSENCE POSTERIOR CERVICAL PLATE SYSTEM - MULTI AXIAL SCREW - NON-STERILE - FDA Registration MDR-10022B

Access comprehensive regulatory information for REBORN ESSENCE POSTERIOR CERVICAL PLATE SYSTEM - MULTI AXIAL SCREW - NON-STERILE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10022B and manufactured by BAUI Biotech Co., Ltd. in Taiwan. The device was registered on July 15, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (EG Healthcare 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.