EVIS LUCERA Colon Videoscope OLYMPUS PCF TYPE Q260AZI - PMDA ID 180590_222ABBZX00130000_A_01_07
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.
Intended for useThis product is intended to observe, diagnose, photograph, and treat the large intestine.
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。