Argo Kit II
Japan·MD·A2106·Updated December 19, 2023- English
- 本品は、聴性脳幹反応の微小な電気信号を児の皮膚を通して検出し、 検査装置に伝えるセンサです。
- 日本語 (Japanese)
- 本品は、聴性脳幹反応の微小な電気信号を児の皮膚を通して検出し、 検査装置に伝えるセンサです。
- Device Type
- MD
- Device Class
- A2106
- Class Name (English)
- Scalp electroencephalogram electrode
- Class Name (日本語)
- 頭皮脳波用電極
- PMDA ID
- 100144_11B1X00002Y21014_3_18_04
- Last Update Date
- December 19, 2023
- Official Documents
- View PDF (PMDA)
- 日本語 (Japanese)
- 製造販売／アトムメディカル株式会社
Access comprehensive regulatory information for Argo Kit II (アルゴキットII) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 100144_11B1X00002Y21014_3_18_04 and manufactured by Manufacturing and sales: Atom Medical Corporation. The device information was last updated on December 19, 2023.
This page provides complete registration details including device class (A2106), classification (Scalp electroencephalogram electrode / 頭皮脳波用電極), manufacturer information (English and Japanese), intended use, 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.