Opti 4 Raparo electrode
Japan·MD·A2900·Updated February 06, 2025- Device Type
- MD
- Device Class
- A2900
- Class Name (English)
- High-frequency treatment active instrument
- Class Name (日本語)
- 高周波処置用能動器具
- PMDA ID
- 610015_302ADBZX00079000_A_01_02
- Last Update Date
- February 06, 2025
- Official Documents
- View PDF (PMDA)
- 日本語 (Japanese)
- 製造販売／コヴィディエンジャパン株式会社
Access comprehensive regulatory information for Opti 4 Raparo electrode (Opti 4ラパロ用電極) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 610015_302ADBZX00079000_A_01_02 and manufactured by Manufacturing and sales: Covidien Japan K.K.. The device information was last updated on February 06, 2025.
This page provides complete registration details including device class (A2900), classification (High-frequency treatment active instrument / 高周波処置用能動器具), 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.