Japan PMDA registration 180590_222ABBZX00130000_A_01_07

EVIS LUCERA Colon Videoscope OLYMPUS PCF TYPE Q260AZI

JP: EVIS LUCERA 大腸ビデオスコープ OLYMPUS PCF TYPE Q260AZI
Japan flagJapan·MD·A2500·Updated September 13, 2022
Intended use / 使用目的
English
Intended for useThis product is intended to observe, diagnose, photograph, and treat the large intestine.
日本語 (Japanese)
使用目的本品は、大腸の観察、診断、撮影、治療を行うことを目的とする。
Device classification / 分類
Device Type
MD
Device Class
A2500
Class Name (English)
video flexible colonoscope
Class Name (日本語)
ビデオ軟性大腸鏡
Registration information / 登録情報
PMDA ID
180590_222ABBZX00130000_A_01_07
Last Update Date
September 13, 2022
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 EVIS LUCERA Colon Videoscope OLYMPUS PCF TYPE Q260AZI (EVIS LUCERA 大腸ビデオスコープ OLYMPUS PCF TYPE Q260AZI) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 180590_222ABBZX00130000_A_01_07 and manufactured by Manufacture and sales/Olympus Medical Systems Corporation. The device information was last updated on September 13, 2022.

This page provides complete registration details including device class (A2500), classification (video flexible colonoscope / ビデオ軟性大腸鏡), manufacturer information (English and Japanese), intended use, 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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