subcutaneous administration set - PMDA ID 530100_22900BZX00413000_A_01_03
Access comprehensive regulatory information for subcutaneous administration set (皮下投与セット) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530100_22900BZX00413000_A_01_03 and manufactured by Nipro Co., Ltd.. The device information was last updated on July 06, 2022.
This page provides complete registration details including device class (A4700), classification (Single use hypodermic needle / 単回使用皮下注射用針), 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.
This product is a set in which medical devices and the like necessary for administering the preparation are combined for improving convenience.
本品は、製剤を投与する際に必要な医療機器等を利便性向上のために組合せたセットである。