Biosense CARTO 3 - PMDA ID 340216_22200BZX00741000_J_01_09

Access comprehensive regulatory information for Biosense CARTO 3 (バイオセンスＣＡＲＴＯ ３) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 340216_22200BZX00741000_J_01_09 and manufactured by Johnson & Johnson Corporation. The device information was last updated on February 05, 2025.

This page provides complete registration details including device class (A2100), classification (Cardiac catheter examination system / 心臓カテーテル用検査装置), 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.