ディスポーザブルホットバイオプシー鉗子 FD-231
Japan·MD·A2500·Updated January 15, 2025- Device Type
- MD
- Device Class
- A2500
- Class Name (English)
- Single-use high-frequency procedure endoscope active instrument
- Class Name (日本語)
- 単回使用高周波処置用内視鏡能動器具
- PMDA ID
- 180590_230ABBZX00055000_A_01_05
- Last Update Date
- January 15, 2025
- Official Documents
- View PDF (PMDA)
- 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
Access comprehensive regulatory information for ディスポーザブルホットバイオプシー鉗子 FD-231 (ディスポーザブルホットバイオプシー鉗子 FD-231) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 180590_230ABBZX00055000_A_01_05 and manufactured by Olympus Medical Systems Corporation. The device information was last updated on January 15, 2025.
This page provides complete registration details including device class (A2500), classification (Single-use high-frequency procedure endoscope active instrument / 単回使用高周波処置用内視鏡能動器具), 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.