Universal Tibia Template 2400319 - PMDA ID 160146_26B2X10004002322_A_01_01

Access comprehensive regulatory information for Universal Tibia Template 2400319 (ユニバーサル脛骨テンプレート 2400319) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 160146_26B2X10004002322_A_01_01 and manufactured by Umihira Corporation. The device information was last updated on October 09, 2024.

This page provides complete registration details including device class (A5800), classification (Joint surgery instrument / 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.