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BD Bactek MGIT 960 - PMDA ID 530513_07B1X00003000123_A_01_03

BD バクテック MGIT 960

Access comprehensive regulatory information for BD Bactek MGIT 960 (BD バクテック MGIT 960) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530513_07B1X00003000123_A_01_03 and manufactured by Manufacture and sales/Nippon Becton Dickinson Co., Ltd.. The device information was last updated on July 01, 2022.

This page provides complete registration details including device class (A2000), classification (Microbial susceptibility analysis device / 微生物感受性分析装置), manufacturer information (English and Japanese), 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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Bilingual (EN/JP)
MD
A2000
530513_07B1X00003000123_A_01_03
MD
A2000
BD Bactek MGIT 960
BD バクテック MGIT 960
PMDA ID: 530513_07B1X00003000123_A_01_03
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Device Classification / 分類
Device Type
MD
Device Class
A2000
Class Name (English)
Microbial susceptibility analysis device
Class Name (日本語)
微生物感受性分析装置
Registration Information / 登録情報
PMDA ID
530513_07B1X00003000123_A_01_03
Last Update Date
July 01, 2022
Official Documents
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/日本ベクトン・ディッキンソン株式会社
Product Names / 製品名
Market Name (English)
BD Bactek MGIT 960
Market Name (日本語)
BD バクテック MGIT 960