AIA-Pack CL FT4II - PMDA ID 480201_13E1X80174002025_A_01_01

Access comprehensive regulatory information for AIA-Pack CL FT4II (ＡＩＡ−パックＣＬ　ＦＴ４ＩＩ) in the Japan medical device market through Pure Global AI's free bilingual database. This IVD medical device is registered under PMDA ID 480201_13E1X80174002025_A_01_01 and manufactured by Tosoh Corporation. The device information was last updated on August 06, 2024.

This page provides complete registration details including device class (IVD), classification (Free thyroxine kit / 遊離サイロキシンキット), 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.