Japan PMDA registration 530100_226AABZX00107000_A_01_07

Nipro Transfusion Set (for Safetech Infusion Pump)

JP: ニプロ輸血セット(セーフテック輸液ポンプ用)
Japan flagJapan·MD·A5600·Updated August 25, 2022
Intended use / 使用目的
English
It is used for the purpose of administering human whole blood products.
日本語 (Japanese)
人全血等血液製剤を投与する目的で使用する。
Device classification / 分類
Device Type
MD
Device Class
A5600
Class Name (English)
transfusion set
Class Name (日本語)
輸血セット
Registration information / 登録情報
PMDA ID
530100_226AABZX00107000_A_01_07
Last Update Date
August 25, 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 Nipro Transfusion Set (for Safetech Infusion Pump) (ニプロ輸血セット(セーフテック輸液ポンプ用)) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530100_226AABZX00107000_A_01_07 and manufactured by Nipro Co., Ltd.. The device information was last updated on August 25, 2022.

This page provides complete registration details including device class (A5600), classification (transfusion set / 輸血セット), 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.

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