BIOMET INTERLOK FIXED CRUCIATE TIBIAL PLATE WITH BAR - FDA Registration MDR-09859A

Access comprehensive regulatory information for BIOMET INTERLOK FIXED CRUCIATE TIBIAL PLATE WITH BAR in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09859A and manufactured by Zimmer Pte. Ltd. in USA. The device was registered on July 02, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Asia Actual Consultancy 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.