Japan PMDA registration 180590_224ABBZX00028000_A_02_12

ENDOEYE FLEX 先端湾曲ビデオスコープ OLYMPUS LTF-S190-10(内視鏡本体)

JP: ENDOEYE FLEX 先端湾曲ビデオスコープ OLYMPUS LTF-S190-10(内視鏡本体)
Japan flagJapan·MD·A2500·Updated February 19, 2025
Device classification / 分類
Device Type
MD
Device Class
A2500
Class Name (English)
videorigid laparoscopy
Class Name (日本語)
ビデオ硬性腹腔鏡
Registration information / 登録情報
PMDA ID
180590_224ABBZX00028000_A_02_12
Last Update Date
February 19, 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 ENDOEYE FLEX 先端湾曲ビデオスコープ OLYMPUS LTF-S190-10(内視鏡本体) (ENDOEYE FLEX 先端湾曲ビデオスコープ OLYMPUS LTF-S190-10(内視鏡本体)) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 180590_224ABBZX00028000_A_02_12 and manufactured by Olympus Medical Systems Corporation. The device information was last updated on February 19, 2025.

This page provides complete registration details including device class (A2500), classification (videorigid laparoscopy / ビデオ硬性腹腔鏡), 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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