HDL Auto "TBA" (N Direct Method) - PMDA ID 470154_15E1X00001000020_A_01_04

Access comprehensive regulatory information for HDL Auto "TBA" (N Direct Method) (ＨＤＬオート「ＴＢＡ」(Ｎ直接法)) in the Japan medical device market through Pure Global AI's free bilingual database. This IVD medical device is registered under PMDA ID 470154_15E1X00001000020_A_01_04 and manufactured by Denka Corporation. The device information was last updated on May 13, 2024.

This page provides complete registration details including device class (IVD), classification (HDL-Cholesterol Kit / ＨＤＬ-コレステロールキット), 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.