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BD MaxTM SARS-CoV-2/Flu - PMDA ID 530513_30400EZX00005000_A_01_01

BD マックスTM SARS-CoV-2/Flu

Access comprehensive regulatory information for BD MaxTM SARS-CoV-2/Flu (BD マックスTM SARS-CoV-2/Flu) in the Japan medical device market through Pure Global AI's free bilingual database. This IVD medical device is registered under PMDA ID 530513_30400EZX00005000_A_01_01 and manufactured by Manufacture and sales/Nippon Becton Dickinson Co., Ltd.. The device information was last updated on March 05, 2022.

This page provides complete registration details including device class (IVD), classification (SARS coronavirus nucleic acid kit / SARSコロナウイルス核酸キット), 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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PMDA Official Data
Bilingual (EN/JP)
IVD
IVD
530513_30400EZX00005000_A_01_01
IVD
IVD
BD MaxTM SARS-CoV-2/Flu
BD マックスTM SARS-CoV-2/Flu
PMDA ID: 530513_30400EZX00005000_A_01_01
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Device Classification / 分類
Device Type
IVD
Device Class
IVD
Class Name (English)
SARS coronavirus nucleic acid kit
Class Name (日本語)
SARSコロナウイルス核酸キット
Registration Information / 登録情報
PMDA ID
530513_30400EZX00005000_A_01_01
Last Update Date
March 05, 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 MaxTM SARS-CoV-2/Flu
Market Name (日本語)
BD マックスTM SARS-CoV-2/Flu