Zenition series - PMDA ID 670277_301AFBZX00026000_A_01_03

Access comprehensive regulatory information for Zenition series (Zenitionシリーズ) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 670277_301AFBZX00026000_A_01_03 and manufactured by Philips Japan Co., Ltd.. The device information was last updated on August 18, 2022.

This page provides complete registration details including device class (A0900), classification (Mobile digital general-purpose integrated X-ray fluoroscopy diagnostic equipment / 移動型デジタル式汎用一体型X線透視診断装置), 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.