Japan PMDA registration 530366_30500BZX00005000_A_01_03

ARES Shunt Catheter

JP: ARES シャント カテーテル
Japan flagJapan·MD·A5100·Updated February 10, 2025
Device classification / 分類
Device Type
MD
Device Class
A5100
Class Name (English)
Cerebrospinal catheter
Class Name (日本語)
脳脊髄用カテーテル
Registration information / 登録情報
PMDA ID
530366_30500BZX00005000_A_01_03
Last Update Date
February 10, 2025
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/日本メドトロニック株式会社
About this record

Access comprehensive regulatory information for ARES Shunt Catheter (ARES シャント カテーテル) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530366_30500BZX00005000_A_01_03 and manufactured by Japan Medtronic Corporation. The device information was last updated on February 10, 2025.

This page provides complete registration details including device class (A5100), classification (Cerebrospinal catheter / 脳脊髄用カテーテル), 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.

Free DatabasePowered by Pure Global AIPMDA Official DataBilingual (EN/JP)MDA5100