Japan PMDA registration 671001_14B1X10022A0K520_A_01_07

FUJIFILM Hood DH-33GR

JP: 富士フイルム フード DH-33GR
Japan flagJapan·MD·A2500·Updated February 03, 2025
Device classification / 分類
Device Type
MD
Device Class
A2500
Class Name (English)
Non-active treatment tool for single-use endoscopy for natural aperture
Class Name (日本語)
自然開口向け単回使用内視鏡用非能動処置具
Registration information / 登録情報
PMDA ID
671001_14B1X10022A0K520_A_01_07
Last Update Date
February 03, 2025
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/富士フイルム株式会社
About this record

Access comprehensive regulatory information for FUJIFILM Hood DH-33GR (富士フイルム フード DH-33GR) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 671001_14B1X10022A0K520_A_01_07 and manufactured by FUJIFILM Corporation. The device information was last updated on February 03, 2025.

This page provides complete registration details including device class (A2500), classification (Non-active treatment tool for single-use endoscopy for natural aperture / 自然開口向け単回使用内視鏡用非能動処置具), 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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