Detaminar L Mg - PMDA ID 530100_27E1X80166000009_A_01_05

Access comprehensive regulatory information for Detaminar L Mg (デタミナーＬ　Ｍｇ) in the Japan medical device market through Pure Global AI's free bilingual database. This IVD medical device is registered under PMDA ID 530100_27E1X80166000009_A_01_05 and manufactured by Nipro Corporation. The device information was last updated on February 01, 2025.

This page provides complete registration details including device class (IVD), classification (Magnesium kit for blood and urine tests / 血液・尿検査用マグネシウムキット), 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.