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Biocube Cannula HCP - PMDA ID 530100_30100BZX00091000_A_01_03

バイオキューブカニューレHCP

Access comprehensive regulatory information for Biocube Cannula HCP (バイオキューブカニューレHCP) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530100_30100BZX00091000_A_01_03 and manufactured by Nipro Corporation. The device information was last updated on February 17, 2025.

This page provides complete registration details including device class (A5100), classification (Heparin-using central circulatory arteriovenous cannula / ヘパリン使用中心循環系動静脈カニューレ), 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
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MD
A5100
530100_30100BZX00091000_A_01_03
MD
A5100
Biocube Cannula HCP
バイオキューブカニューレHCP
PMDA ID: 530100_30100BZX00091000_A_01_03
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Device Classification / 分類
Device Type
MD
Device Class
A5100
Class Name (English)
Heparin-using central circulatory arteriovenous cannula
Class Name (日本語)
ヘパリン使用中心循環系動静脈カニューレ
Registration Information / 登録情報
PMDA ID
530100_30100BZX00091000_A_01_03
Last Update Date
February 17, 2025
Official Documents
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/ニプロ株式会社
Product Names / 製品名
Market Name (English)
Biocube Cannula HCP
Market Name (日本語)
バイオキューブカニューレHCP