Artemis Programmer - PMDA ID 381005_22900BZX00175000_B_01_08
Access comprehensive regulatory information for Artemis Programmer (Artemis プログラマ) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 381005_22900BZX00175000_B_01_08 and manufactured by Manufacture and sales / Abbott Medical Japan G.K.. The device information was last updated on January 07, 2022.
This page provides complete registration details including device class (A1200), classification (Programmer for implantable active devices / 植込み能動型機器用プログラマ), 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.
For < intended use> this product is used to non-invasively change one or more electrical actuation characteristics of a particular Abbott implantable pulse generator or extracorporeal pulse generator. 1/5 Programmer for implantable active devices 70586000 (Parameter selection program for electrical stimulation therapy device 71051003) Programmer patient controller)
＜使用目的＞本品は、特定のAbbott社製の植込み型パルスジェネレータ又は体外式パルスジェネレータの有する1つ以上の電気作動特性を非侵襲的に変化させるのに用いる。1/5植込み能動型機器用プログラマ 70586000（電気刺激治療装置用パラメータ選択プログラム 71051003）プログラマ患者用コントローラ）