Japan PMDA registration 170163_13B1X00218258041_A_01_03

bone mill set

JP: ボーンミルセット
Japan flagJapan·MD·A5800·Updated February 25, 2022
Intended use / 使用目的
English
This product is used in orthopedic surgery. It is an instrument used to pulverize bone for use as a bone matrix for bone regeneration or bone grafting.
日本語 (Japanese)
本品は、整形外科手術において使用する。骨再生又は骨移植用の骨基質として用いるために骨を粉砕するのに用いる器具である。
Device classification / 分類
Device Type
MD
Device Class
A5800
Class Name (English)
bone mill
Class Name (日本語)
ボーンミル
Registration information / 登録情報
PMDA ID
170163_13B1X00218258041_A_01_03
Last Update Date
February 25, 2022
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/ビー・ブラウンエースクラップ株式会社
About this record

Access comprehensive regulatory information for bone mill set (ボーンミルセット) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 170163_13B1X00218258041_A_01_03 and manufactured by Manufacture and sales / B.Brown Ace scrap Co., Ltd.. The device information was last updated on February 25, 2022.

This page provides complete registration details including device class (A5800), classification (bone mill / ボーンミル), 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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