Angioline - PMDA ID 250037_20400BZZ00927000_A_01_09

Access comprehensive regulatory information for Angioline (アンギオライン) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 250037_20400BZZ00927000_A_01_09 and manufactured by Manufacturing and sales: Create Medic Corporation. The device information was last updated on October 02, 2024.

This page provides complete registration details including device class (A5100), classification (Angiography kit / 血管造影キット), 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.