FARASTAR CONSOLE - PMDA ID 300500_30600BZX00196000_A_01_01

Access comprehensive regulatory information for FARASTAR CONSOLE (FARASTAR コンソール) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 300500_30600BZX00196000_A_01_01 and manufactured by Boston Scientific Japan K.K.. The device information was last updated on October 04, 2024.

This page provides complete registration details including device class (A2900), classification (Percutaneous myocardial ablation electrosurgical unit / 経皮心筋焼灼術用電気手術ユニット), 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.