Nipro Transfusion Set (for Safetech Infusion Pump) - PMDA ID 530100_226AABZX00107000_A_01_07
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.
It is used for the purpose of administering human whole blood products.
人全血等血液製剤を投与する目的で使用する。