Japan PMDA registration 100812_28B3X10030JMA101_A_01_01

内方化プッシャー45°

JP: 内方化プッシャー45°
Japan flagJapan·MD·A5800·Updated January 30, 2025
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
100812_28B3X10030JMA101_A_01_01
Last Update Date
January 30, 2025
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/アリオメディカル株式会社
About this record

Access comprehensive regulatory information for 内方化プッシャー45° (内方化プッシャー45°) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 100812_28B3X10030JMA101_A_01_01 and manufactured by Ario Medical Corporation. The device information was last updated on January 30, 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.

Free DatabasePowered by Pure Global AIPMDA Official DataBilingual (EN/JP)MDA5800