BIOMET® KNEE SYSTEM MODULAR TIBIAL AUGMENTATION BLOCK ML/LL WITH SCREWS - FDA Registration MDR-09920B

Access comprehensive regulatory information for BIOMET® KNEE SYSTEM MODULAR TIBIAL AUGMENTATION BLOCK ML/LL WITH SCREWS in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09920B 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.