Concorde CFRP I/Fケージ
Japan·MD·B0400·Updated February 19, 2025- Device Type
- MD
- Device Class
- B0400
- Class Name (English)
- Spinal cage
- Class Name (日本語)
- 脊椎ケージ
- PMDA ID
- 340216_22200BZX00806000_A_01_03
- Last Update Date
- February 19, 2025
- Official Documents
- View PDF (PMDA)
- 日本語 (Japanese)
- 製造販売／ジョンソン・エンド・ジョンソン株式会社
Access comprehensive regulatory information for Concorde CFRP I/Fケージ (Concorde CFRP I/Fケージ) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 340216_22200BZX00806000_A_01_03 and manufactured by Johnson & Johnson Corporation. The device information was last updated on February 19, 2025.
This page provides complete registration details including device class (B0400), classification (Spinal cage / 脊椎ケージ), 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.