Aquamantis Bipolar Sealer - PMDA ID 530366_302ADBZX00057000_A_01_02

Access comprehensive regulatory information for Aquamantis Bipolar Sealer (アクアマンティス・バイポーラシーラー) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530366_302ADBZX00057000_A_01_02 and manufactured by Medtronic Japan Co., Ltd.. The device information was last updated on October 17, 2022.

This page provides complete registration details including device class (A2900), classification (bipolar electrode / バイポーラ電極), 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.