Aquamantis Bipolar Sealer
Japan·MD·A2900·Updated October 17, 2022- Device Type
- MD
- Device Class
- A2900
- Class Name (English)
- bipolar electrode
- Class Name (日本語)
- バイポーラ電極
- PMDA ID
- 530366_302ADBZX00057000_A_01_02
- Last Update Date
- October 17, 2022
- Official Documents
- View PDF (PMDA)
- English
- Medtronic Japan Co., Ltd.
- 日本語 (Japanese)
- 製造販売／日本メドトロニック株式会社
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.