Cardiosoft ECG - PMDA ID 530979_21600BZY00488000_A_01_12

Access comprehensive regulatory information for Cardiosoft ECG (カーディオソフト　ＥＣＧ) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530979_21600BZY00488000_A_01_12 and manufactured by GE Healthcare Japan K.K.. The device information was last updated on January 06, 2025.

This page provides complete registration details including device class (A2100), classification (General-purpose electrocardiograph / 汎用心電計), manufacturer information (English and Japanese), 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.