hammer - PMDA ID 510462_33B1X100010D0040_A_01_01

Access comprehensive regulatory information for hammer (ハンマー) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 510462_33B1X100010D0040_A_01_01 and manufactured by Teijin Nakashima Medical Corporation. The device information was last updated on January 09, 2025.

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.