encore pro 2 - PMDA ID 670277_22800BZX00006000_A_02_04
Access comprehensive regulatory information for encore pro 2 (アンコールプロ2) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 670277_22800BZX00006000_A_02_04 and manufactured by Philips Japan Co., Ltd.. The device information was last updated on October 04, 2022.
This page provides complete registration details including device class (E0200), classification (Respiratory therapy support program / 呼吸装置治療支援プログラム), 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 program is used by physicians to centrally manage patient information and treatment information such as ventilators used at home and in hospitals on personal computers. In addition, doctors can change the prescription (setting parameters) of ventilators, etc. through this program via SD card (or smart card).
本プログラムは、医師がパーソナルコンピュータ上で、在宅及び院内で使用される人工呼吸器等の患者情報及び治療情報を集中管理するために使用される。また、医師はSDカード（またはスマートカード）を介して、本プログラムにより人工呼吸器等の処方（設定パラメータ）を変更できる。