ARES Shunt Catheter - PMDA ID 530366_30500BZX00005000_A_01_03

Access comprehensive regulatory information for ARES Shunt Catheter (ARES シャント カテーテル) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530366_30500BZX00005000_A_01_03 and manufactured by Japan Medtronic Corporation. The device information was last updated on February 10, 2025.

This page provides complete registration details including device class (A5100), classification (Cerebrospinal catheter / 脳脊髄用カテーテル), 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.