Cobus T System Fibrinogen - PMDA ID 700025_13E1X80206000158_A_02_04

Access comprehensive regulatory information for Cobus T System Fibrinogen (コバス　t　システム　フィブリノーゲン) in the Japan medical device market through Pure Global AI's free bilingual database. This IVD medical device is registered under PMDA ID 700025_13E1X80206000158_A_02_04 and manufactured by Roche Diagnostics K.K.. The device information was last updated on February 19, 2025.

This page provides complete registration details including device class (IVD), classification (Fibrinogen Kit / フィブリノーゲンキット), 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.