OM Femoral Rasp - PMDA ID 180535_25B1X00002000211_A_01_01
Access comprehensive regulatory information for OM Femoral Rasp (OM Femoral ラスプ) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 180535_25B1X00002000211_A_01_01 and manufactured by Ohmic Co., Ltd.. The device information was last updated on December 08, 2021.
This page provides complete registration details including device class (A5800), classification (joint surgery instruments / 関節手術用器械), manufacturer information (English and Japanese), intended use, 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.
・This product refers to surgical instruments used for joint surgery such as artificial joint replacement. Limited to manual types. This product is reusable.
・本品は、人工関節置換術等の関節手術に用いる手術器械をいう。手動式のものに限る。本品は再使用可能である。