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BD Max CDIFF - PMDA ID 530513_22800EZX00002000_A_01_02

BD マックス CDIFF

Access comprehensive regulatory information for BD Max CDIFF (BD マックス CDIFF) in the Japan medical device market through Pure Global AI's free bilingual database. This IVD medical device is registered under PMDA ID 530513_22800EZX00002000_A_01_02 and manufactured by Manufacture and sales/Nippon Becton Dickinson Co., Ltd.. The device information was last updated on July 15, 2022.

This page provides complete registration details including device class (IVD), classification (Clostridium difficile nucleic acid kit / クロストリジウム・ディフィシル核酸キット), 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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PMDA Official Data
Bilingual (EN/JP)
IVD
IVD
530513_22800EZX00002000_A_01_02
IVD
IVD
BD Max CDIFF
BD マックス CDIFF
PMDA ID: 530513_22800EZX00002000_A_01_02
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Intended Use / 使用目的
English

DNA detection of Clostridium difficile toxin B in feces (Clostridium

日本語 (Japanese)

糞便中のClostridium difficile トキシンBのDNA検出(Clostridium

Device Classification / 分類
Device Type
IVD
Device Class
IVD
Class Name (English)
Clostridium difficile nucleic acid kit
Class Name (日本語)
クロストリジウム・ディフィシル核酸キット
Registration Information / 登録情報
PMDA ID
530513_22800EZX00002000_A_01_02
Last Update Date
July 15, 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 Max CDIFF
Market Name (日本語)
BD マックス CDIFF