Cobus BRAF V600 Mutation Detection Kit - PMDA ID 700025_22600AMX01329000_A_01_06

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.