Ektra II System - PMDA ID 371113_20400BZY00450000_A_04_03

Access comprehensive regulatory information for Ektra II System (エクトラＩＩ　システム) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 371113_20400BZY00450000_A_04_03 and manufactured by Smith & Nephew Corporation. The device information was last updated on October 02, 2024.

This page provides complete registration details including device class (A2500), classification (Rigid arthroscope / 硬性関節鏡), 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.