Japan PMDA registration 160146_26B2X10004002322_A_01_01

Universal Tibia Template 2400319

JP: ユニバーサル脛骨テンプレート 2400319

Japan·MD·A5800·Updated October 09, 2024

Device classification / 分類

Device Type: MD
Device Class: A5800
Class Name (English): Joint surgery instrument
Class Name (日本語): 関節手術用器械

Registration information / 登録情報

PMDA ID: 160146_26B2X10004002322_A_01_01
Last Update Date: October 09, 2024
Official Documents: View PDF (PMDA)

Manufacturer / 製造販売業者

English: Umihira Corporation
日本語 (Japanese): 製造販売／株式会社ウミヒラ

About this record

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.

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