Espa AMY Liquid II - PMDA ID 530100_21300AMZ00421000_A_01_04

Access comprehensive regulatory information for Espa AMY Liquid II (エスパ・ＡＭＹリキッドII) in the Japan medical device market through Pure Global AI's free bilingual database. This IVD medical device is registered under PMDA ID 530100_21300AMZ00421000_A_01_04 and manufactured by Nipro Co., Ltd.. The device information was last updated on January 26, 2022.

This page provides complete registration details including device class (IVD), classification (amylase kit / アミラーゼキット), 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.