AIA-Pack CL SARS-CoV-2-Ag
Japan·IVD·IVD·Updated May 30, 2024- Device Type
- IVD
- Device Class
- IVD
- Class Name (English)
- SARS Coronavirus Antigen Kit
- Class Name (日本語)
- SARSコロナウイルス抗原キット
- PMDA ID
- 480201_30300EZX00075000_A_01_05
- Last Update Date
- May 30, 2024
- Official Documents
- View PDF (PMDA)
- English
- Tosoh Corporation
- 日本語 (Japanese)
- 製造販売／東ソー株式会社
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.