Iatro LQ GLU (7L-61K2, 710-61K2, LS8-61K2, TBA-61K2) - PMDA ID 530100_27E1X80166000006_A_01_02

Access comprehensive regulatory information for Iatro LQ GLU (7L-61K2, 710-61K2, LS8-61K2, TBA-61K2) (イアトロＬＱ　ＧＬＵ　（７Ｌ−６１Ｋ２、７１０−６１Ｋ２、ＬＳ８−６１Ｋ２、ＴＢＡ−６１Ｋ２）) in the Japan medical device market through Pure Global AI's free bilingual database. This IVD medical device is registered under PMDA ID 530100_27E1X80166000006_A_01_02 and manufactured by Nipro Co., Ltd.. The device information was last updated on April 14, 2021.

This page provides complete registration details including device class (IVD), classification (Glucose kit for blood and urine tests / 血液・尿検査用グルコースキット), 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.