PENTAXMedical内視鏡用把持鉗子VDK-FG
Japan·MD·A2500·Updated July 04, 2024- 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
- PMDA ID
- 710098_13B1X00253800075_A_01_04
- Last Update Date
- July 04, 2024
- Official Documents
- View PDF (PMDA)
- English
- HOYA Corporation
- 日本語 (Japanese)
- 製造販売／HOYA株式会社
Access comprehensive regulatory information for PENTAXMedical内視鏡用把持鉗子VDK-FG (PENTAXMedical内視鏡用把持鉗子VDK-FG) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 710098_13B1X00253800075_A_01_04 and manufactured by HOYA Corporation. The device information was last updated on July 04, 2024.
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.