Meira (forceps) - PMDA ID 510173_21B1X00003000080_A_01_04

Access comprehensive regulatory information for Meira (forceps) (メイラ(鉗子)) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 510173_21B1X00003000080_A_01_04 and manufactured by Meira Corporation. The device information was last updated on August 13, 2024.

This page provides complete registration details including device class (A5800), classification (Orthopedic fixed forceps / 整形外科用固定鉗子), 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.