head trial
Japan·MD·A5800·Updated October 21, 2022- Device Type
- MD
- Device Class
- A5800
- Class Name (English)
- joint surgery instruments
- Class Name (日本語)
- 関節手術用器械
- PMDA ID
- 670399_29B2X10008ZIB011_A_01_18
- Last Update Date
- October 21, 2022
- Official Documents
- View PDF (PMDA)
- 日本語 (Japanese)
- 製造販売／株式会社フジフレックス
Access comprehensive regulatory information for head trial (ヘッドトライアル) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 670399_29B2X10008ZIB011_A_01_18 and manufactured by Manufacture and sales/Fujiflex Co., Ltd.. The device information was last updated on October 21, 2022.
This page provides complete registration details including device class (A5800), classification (joint surgery instruments / 関節手術用器械), 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.