若年者FemガイドIII
Japan·MD·A5800·Updated February 04, 2025- Device Type
- MD
- Device Class
- A5800
- Class Name (English)
- Ligament and tendon surgery instrument
- Class Name (日本語)
- 靭帯・腱手術用器械
- PMDA ID
- 100812_28B3X10030AI3459_A_01_01
- Last Update Date
- February 04, 2025
- Official Documents
- View PDF (PMDA)
- English
- Ario Medical Corporation
- 日本語 (Japanese)
- 製造販売／アリオメディカル株式会社
Access comprehensive regulatory information for 若年者FemガイドIII (若年者FemガイドIII) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 100812_28B3X10030AI3459_A_01_01 and manufactured by Ario Medical Corporation. The device information was last updated on February 04, 2025.
This page provides complete registration details including device class (A5800), classification (Ligament and tendon surgery instrument / 靭帯・腱手術用器械), 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.