RE file - PMDA ID 830029_301ALBZX00015000_A_01_04
Access comprehensive regulatory information for RE file (ＲＥ ファイル) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 830029_301ALBZX00015000_A_01_04 and manufactured by Yoshida Co., Ltd.. The device information was last updated on March 01, 2021.
This page provides complete registration details including device class (A4913), classification (electric dental file / 電動式歯科用ファイル), 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.
In order to enlarge the root canal or smooth the root canal wall, it is connected to an active device and used for cutting or polishing by making a reciprocating motion or pulling up and down direction.
根管の拡大又は根管壁を平滑にするため、能動型機器に接続 し、これに上下方向の往復運動又は引上げ動作をさせることによる切削又は研磨に用いる。