RI KNEEティビアルフィグゼーションベース / SM - PMDA ID 260148_22B3X00005SN0120_Z_01_01

Access comprehensive regulatory information for RI KNEEティビアルフィグゼーションベース / SM (RI KNEEティビアルフィグゼーションベース / SM) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 260148_22B3X00005SN0120_Z_01_01 and manufactured by KSI Corporation. The device information was last updated on February 07, 2025.

This page provides complete registration details including device class (A5800), classification (Joint surgery instrument / 関節手術用器械), manufacturer information (English and Japanese), and regulatory compliance data from the official Japan PMDA medical device database. Pure Global AI offers free bilingual access to Japan's complete medical device registry, helping global MedTech companies navigate PMDA regulations efficiently.