POLAR SYSTEM LATERAL Ti/HA, NON-CEMENTED - FDA Registration MDR-05052B

Access comprehensive regulatory information for POLAR SYSTEM LATERAL Ti/HA, NON-CEMENTED in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05052B and manufactured by Smith & Nephew Pte. Limited in Switzerland. The device was registered on January 23, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (RBGM Medical Express Sales, 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.