Nipro IP Echo - PMDA ID 530100_230AABZX00103000_A_01_03
Access comprehensive regulatory information for Nipro IP Echo (ニプロＩＰエコー) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530100_230AABZX00103000_A_01_03 and manufactured by Nipro Co., Ltd.. The device information was last updated on December 02, 2021.
This page provides complete registration details including device class (A1200), classification (General-purpose ultrasound imaging system / 汎用超音波画像診断装置), manufacturer information (English and Japanese), intended use, 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.
This product is a device that visualizes an ultrasonic tomography image in the body based on the ultrasonic pulse reflection method for diagnosis. <Precautions for use or effects>1. This product is not intended for direct application to the heart.
本品は、診断のために、超音波パルス反射法に基づき、体内の超音波断層像を描出する装置である。＜使用目的又は効果に関する使用上の注意＞1.本品は心臓への直接適用を意図していない。