Japan PMDA registration 340216_227ADBZX00135000_A_01_03

Shoulder prosthesis, single-use surgical instrument

JP: 人工肩関節用単回使用手術器械
Japan flagJapan·MD·A5800·Updated February 14, 2025
Device classification / 分類
Device Type
MD
Device Class
A5800
Class Name (English)
Single-use joint surgery instrument
Class Name (日本語)
単回使用関節手術用器械
Registration information / 登録情報
PMDA ID
340216_227ADBZX00135000_A_01_03
Last Update Date
February 14, 2025
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/ジョンソン・エンド・ジョンソン株式会社
About this record

Access comprehensive regulatory information for Shoulder prosthesis, single-use surgical instrument (人工肩関節用単回使用手術器械) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 340216_227ADBZX00135000_A_01_03 and manufactured by Johnson & Johnson Corporation. The device information was last updated on February 14, 2025.

This page provides complete registration details including device class (A5800), classification (Single-use joint surgery instrument / 単回使用関節手術用器械), 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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