Japan PMDA registration 530100_16100BZZ01735000_S_02_08

Blood Access UK-Catheter Kit (Triple Lumen Catheter Safety Y Connector Type/Full Kit Type)

JP: ブラッドアクセス UK−カテーテルキット(トリプルルーメンカテーテル セーフティYコネクタタイプ/フルキットタイプ)
Japan flagJapan·MD·A5100·Updated January 08, 2025
Device classification / 分類
Device Type
MD
Device Class
A5100
Class Name (English)
Urokinase-based emergency blood access indwelling catheter
Class Name (日本語)
ウロキナーゼ使用緊急時ブラッドアクセス留置用カテーテル
Registration information / 登録情報
PMDA ID
530100_16100BZZ01735000_S_02_08
Last Update Date
January 08, 2025
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/ニプロ株式会社
About this record

Access comprehensive regulatory information for Blood Access UK-Catheter Kit (Triple Lumen Catheter Safety Y Connector Type/Full Kit Type) (ブラッドアクセス UK−カテーテルキット(トリプルルーメンカテーテル セーフティYコネクタタイプ/フルキットタイプ)) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530100_16100BZZ01735000_S_02_08 and manufactured by Nipro Corporation. The device information was last updated on January 08, 2025.

This page provides complete registration details including device class (A5100), classification (Urokinase-based emergency blood access indwelling catheter / ウロキナーゼ使用緊急時ブラッドアクセス留置用カテーテル), 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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