Japan PMDA registration 510173_21B1X00003000080_A_01_04

Meira (forceps)

JP: メイラ(鉗子)
Japan flagJapan·MD·A5800·Updated August 13, 2024
Device classification / 分類
Device Type
MD
Device Class
A5800
Class Name (English)
Orthopedic fixed forceps
Class Name (日本語)
整形外科用固定鉗子
Registration information / 登録情報
PMDA ID
510173_21B1X00003000080_A_01_04
Last Update Date
August 13, 2024
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/メイラ株式会社
About this record

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.

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