Link® Polyethylene Articular Surface Fixed Bearing PS Gemini® SL® Total Knee Replacement, Left

Access comprehensive regulatory information for Link® Polyethylene Articular Surface Fixed Bearing PS Gemini® SL® Total Knee Replacement, Left in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04513 and manufactured by Walder Link GmbH & Co. KG. Barkhausenweg 10, 22339 Hamburg, Germany in Germany. The device was registered on May 23, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (Westech Meditrade, 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.