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Anteauru WR - PMDA ID 470034_22900BZX00096000_A_01_02

アンテアウルWR

Access comprehensive regulatory information for Anteauru WR (アンテアウルWR) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 470034_22900BZX00096000_A_01_02 and manufactured by Terumo Corporation. The device information was last updated on October 20, 2022.

This page provides complete registration details including device class (A5100), classification (Central Circulatory Intravascular Ultrasound Catheter / 中心循環系血管内超音波カテーテル), 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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MD
A5100
470034_22900BZX00096000_A_01_02
MD
A5100
Anteauru WR
アンテアウルWR
PMDA ID: 470034_22900BZX00096000_A_01_02
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Device Classification / 分類
Device Type
MD
Device Class
A5100
Class Name (English)
Central Circulatory Intravascular Ultrasound Catheter
Class Name (日本語)
中心循環系血管内超音波カテーテル
Registration Information / 登録情報
PMDA ID
470034_22900BZX00096000_A_01_02
Last Update Date
October 20, 2022
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)
Anteauru WR
Market Name (日本語)
アンテアウルWR