Cobus BRAF V600 Mutation Detection Kit
Japan·IVD·IVD·Updated February 14, 2025- Device Type
- IVD
- Device Class
- IVD
- Class Name (English)
- BRAF Gene Mutation Detection Kit
- Class Name (日本語)
- BRAF 遺伝子変異検出キット
- PMDA ID
- 700025_22600AMX01329000_A_01_06
- Last Update Date
- February 14, 2025
- Official Documents
- View PDF (PMDA)
- English
- Roche Diagnostics K.K.
- 日本語 (Japanese)
- 製造販売／ロシュ・ダイアグノスティックス株式会社
Access comprehensive regulatory information for Cobus BRAF V600 Mutation Detection Kit (コバス BRAF V600 変異検出キット) in the Japan medical device market through Pure Global AI's free bilingual database. This IVD medical device is registered under PMDA ID 700025_22600AMX01329000_A_01_06 and manufactured by Roche Diagnostics K.K.. The device information was last updated on February 14, 2025.
This page provides complete registration details including device class (IVD), classification (BRAF Gene Mutation Detection Kit / BRAF 遺伝子変異検出キット), 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.