ECIF P system side pusher - PMDA ID 750054_13B1X00306G11203_A_01_01
Access comprehensive regulatory information for ECIF P system side pusher (ＥＣＩＦ Ｐシステム サイドプッシャー) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 750054_13B1X00306G11203_A_01_01 and manufactured by Manufacture and sales/Mizuho Co., Ltd.. The device information was last updated on September 15, 2022.
This page provides complete registration details including device class (A5800), classification (Instruments for spine surgery / 脊椎手術用器械), 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 a surgical instrument used for spinal surgery such as spinal fusion. Limited to manual types. This product is reusable.
本品は、脊椎固定術等の脊椎手術のため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。