Ｃ２−９−Ｄプローブ(Ｃ２−９−Ｄプローブ／Ｃ２−９ＶＮ−Ｄプローブ／Ｃ２−９−ＲＳプローブ)

Access comprehensive regulatory information for Ｃ２−９−Ｄプローブ(Ｃ２−９−Ｄプローブ／Ｃ２−９ＶＮ−Ｄプローブ／Ｃ２−９−ＲＳプローブ) (Ｃ２−９−Ｄプローブ（Ｃ２−９−Ｄプローブ／Ｃ２−９ＶＮ−Ｄプローブ／Ｃ２−９−ＲＳプローブ）) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530979_224ABBZX00142000_A_01_09 and manufactured by GE Healthcare Japan K.K.. The device information was last updated on October 07, 2024.

This page provides complete registration details including device class (A1200), classification (Hand-heldextracorporeal ultrasound probe / 手持型体外式超音波診断用プローブ), 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.