PENTAXMedical内視鏡用生検鉗子VDK-FB - PMDA ID 710098_13B1X00253800073_A_01_04

Access comprehensive regulatory information for PENTAXMedical内視鏡用生検鉗子VDK-FB (PENTAXMedical内視鏡用生検鉗子VDK-FB) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 710098_13B1X00253800073_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.