AIA-Pack CL SARS-CoV-2-Ag - PMDA ID 480201_30300EZX00075000_A_01_05

Access comprehensive regulatory information for AIA-Pack CL SARS-CoV-2-Ag (ＡＩＡ−パックＣＬ　ＳＡＲＳ−ＣｏＶ−２−Ａｇ) in the Japan medical device market through Pure Global AI's free bilingual database. This IVD medical device is registered under PMDA ID 480201_30300EZX00075000_A_01_05 and manufactured by Tosoh Corporation. The device information was last updated on May 30, 2024.

This page provides complete registration details including device class (IVD), classification (SARS Coronavirus Antigen Kit / SARSコロナウイルス抗原キット), 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.