Japan PMDA registration 750054_13B1X00306G11202_A_01_01

Deep flexible spatula SUS

JP: 深部柔軟性脳箆 SUS
Japan flagJapan·MD·A5000·Updated June 20, 2022
Intended use / 使用目的
English
This product refers to a surgical instrument used to separate tissue or other anatomical parts. Examination or treatment is possible by exposure or access of organs or tissues. This product is reusable.
日本語 (Japanese)
本品は、組織又は他の解剖学的部位を分離するために用いる手術器具をいう。臓器又は組織の露出やアクセスによって検査又は治療を可能にする。本品は再使用可能である。
Device classification / 分類
Device Type
MD
Device Class
A5000
Class Name (English)
pioneer
Class Name (日本語)
開創器
Registration information / 登録情報
PMDA ID
750054_13B1X00306G11202_A_01_01
Last Update Date
June 20, 2022
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/ミズホ株式会社
About this record

Access comprehensive regulatory information for Deep flexible spatula SUS (深部柔軟性脳箆 SUS) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 750054_13B1X00306G11202_A_01_01 and manufactured by Manufacture and sales/Mizuho Co., Ltd.. The device information was last updated on June 20, 2022.

This page provides complete registration details including device class (A5000), classification (pioneer / 開創器), 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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