Postolateral fibone-lateral template
Japan·MD·A5800·Updated October 15, 2024- Device Type
- MD
- Device Class
- A5800
- Class Name (English)
- Bone surgery instrument
- Class Name (日本語)
- 骨手術用器械
- PMDA ID
- 201618_27B2X00329240317_A_01_01
- Last Update Date
- October 15, 2024
- Official Documents
- View PDF (PMDA)
- English
- Medmetalex Corporation
- 日本語 (Japanese)
- 製造販売／株式会社 メドメタレックス
Access comprehensive regulatory information for Postolateral fibone-lateral template (腓骨後外側テンプレート) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 201618_27B2X00329240317_A_01_01 and manufactured by Medmetalex Corporation. The device information was last updated on October 15, 2024.
This page provides complete registration details including device class (A5800), classification (Bone surgery instrument / 骨手術用器械), 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.