Japan PMDA registration 180590_231ABBZX00016000_A_01_07

Disposable APU Probes

JP: ディスポーザブルAPUプローブ
Japan flagJapan·MD·A2900·Updated February 12, 2025
Device classification / 分類
Device Type
MD
Device Class
A2900
Class Name (English)
Active instrument for combined substance treatment
Class Name (日本語)
物質併用処置用能動器具
Registration information / 登録情報
PMDA ID
180590_231ABBZX00016000_A_01_07
Last Update Date
February 12, 2025
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/オリンパスメディカルシステムズ株式会社
About this record

Access comprehensive regulatory information for Disposable APU Probes (ディスポーザブルAPUプローブ) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 180590_231ABBZX00016000_A_01_07 and manufactured by Olympus Medical Systems Corporation. The device information was last updated on February 12, 2025.

This page provides complete registration details including device class (A2900), classification (Active instrument for combined substance treatment / 物質併用処置用能動器具), 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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