Japan PMDA registration 530100_21300AMZ00421000_A_01_04

Espa AMY Liquid II

JP: エスパ・AMYリキッドII
Japan flagJapan·IVD·IVD·Updated January 26, 2022
Device classification / 分類
Device Type
IVD
Device Class
IVD
Class Name (English)
amylase kit
Class Name (日本語)
アミラーゼキット
Registration information / 登録情報
PMDA ID
530100_21300AMZ00421000_A_01_04
Last Update Date
January 26, 2022
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/ニプロ株式会社
About this record

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.

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