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RelayPro Chest Stent Graft System - PMDA ID 470034_30300BZX00323000_A_01_04

RelayPro 胸部ステントグラフトシステム

Access comprehensive regulatory information for RelayPro Chest Stent Graft System (RelayPro 胸部ステントグラフトシステム) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 470034_30300BZX00323000_A_01_04 and manufactured by Manufacture and sale: Terumo Corporation. The device information was last updated on January 15, 2025.

This page provides complete registration details including device class (A0700), classification (Aortic stent graft / 大動脈用ステントグラフト), 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)
MD
A0700
470034_30300BZX00323000_A_01_04
MD
A0700
RelayPro Chest Stent Graft System
RelayPro 胸部ステントグラフトシステム
PMDA ID: 470034_30300BZX00323000_A_01_04
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Device Classification / 分類
Device Type
MD
Device Class
A0700
Class Name (English)
Aortic stent graft
Class Name (日本語)
大動脈用ステントグラフト
Registration Information / 登録情報
PMDA ID
470034_30300BZX00323000_A_01_04
Last Update Date
January 15, 2025
Official Documents
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/テルモ株式会社
Product Names / 製品名
Market Name (English)
RelayPro Chest Stent Graft System
Market Name (日本語)
RelayPro 胸部ステントグラフトシステム