BD Bactek MGIT 960
Japan·MD·A2000·Updated July 01, 2022- 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
- PMDA ID
- 530513_07B1X00003000123_A_01_03
- Last Update Date
- July 01, 2022
- Official Documents
- View PDF (PMDA)
- 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
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.