Ektra II surgical instrument - PMDA ID 371113_13B1X10222SD0036_A_01_01

Access comprehensive regulatory information for Ektra II surgical instrument (エクトラII手術器械) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 371113_13B1X10222SD0036_A_01_01 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 (Reusable non-active endoscopic tool / 再使用可能な内視鏡用非能動処置具), 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.