Japan PMDA registration 770036_229AHBZX00042000_A_01_02

MMI resuscitation bag Rescu-6

JP: MMI蘇生バッグRescu-6
Japan flagJapan·MD·A0600·Updated July 12, 2022
Intended use / 使用目的
English
Use for air or auxiliary ventilation. It is a single-use manual device.
日本語 (Japanese)
気または補助換気に用いる。単回使用の手動式装置である。
Device classification / 分類
Device Type
MD
Device Class
A0600
Class Name (English)
single use manual pulmonary resuscitator
Class Name (日本語)
単回使用手動式肺人工蘇生器
Registration information / 登録情報
PMDA ID
770036_229AHBZX00042000_A_01_02
Last Update Date
July 12, 2022
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/村中医療器株式会社
About this record

Access comprehensive regulatory information for MMI resuscitation bag Rescu-6 (MMI蘇生バッグRescu-6) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 770036_229AHBZX00042000_A_01_02 and manufactured by Muranaka Medical Instruments Co., Ltd.. The device information was last updated on July 12, 2022.

This page provides complete registration details including device class (A0600), classification (single use manual pulmonary resuscitator / 単回使用手動式肺人工蘇生器), 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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