PENTAXMedical内視鏡用高周波スネアVDK-SD - PMDA ID 710098_302AGBZX00093000_A_01_03

Access comprehensive regulatory information for PENTAXMedical内視鏡用高周波スネアVDK-SD (PENTAXMedical内視鏡用高周波スネアVDK-SD) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 710098_302AGBZX00093000_A_01_03 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 (Single-use electrosurgical endoscope snare / 単回使用電気手術向け内視鏡用スネア), 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.