Japan PMDA registration 530100_27B1X00045000110_A_01_04

Saliva Amylase Monitor

JP: 唾液アミラーゼモニター
Japan flagJapan·MD·A1700·Updated August 28, 2024
Device classification / 分類
Device Type
MD
Device Class
A1700
Class Name (English)
Dry clinical chemistry analyzer
Class Name (日本語)
乾式臨床化学分析装置
Registration information / 登録情報
PMDA ID
530100_27B1X00045000110_A_01_04
Last Update Date
August 28, 2024
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 Saliva Amylase Monitor (唾液アミラーゼモニター) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530100_27B1X00045000110_A_01_04 and manufactured by Nipro Corporation. The device information was last updated on August 28, 2024.

This page provides complete registration details including device class (A1700), classification (Dry clinical chemistry analyzer / 乾式臨床化学分析装置), 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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