PreciTotal PreciTotal Knee System - Femoral Component, Hi-Flex - FDA Registration CMDR-2023-01374A

Access comprehensive regulatory information for PreciTotal PreciTotal Knee System - Femoral Component, Hi-Flex in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2023-01374A and manufactured by AAP Joints GmbH Wilhelm-von-Siemens-Str. 23, Aufgang F, 12277 Berlin, Germany Mfd. By: Youshi Medical Suzhou Co., Ltd. 1&2F Building 2 South No. 188 Jianglingjiang, Suzhou City, Jiangsu Province,215163, P.R. China in Germany. The device was registered on April 05, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (Somnotec Philippines, 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.