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引きドリルII用ガイド - PMDA ID 100812_28B3X10030SNA010_A_01_01

引きドリルII用ガイド

Access comprehensive regulatory information for 引きドリルII用ガイド (引きドリルII用ガイド) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 100812_28B3X10030SNA010_A_01_01 and manufactured by Ario Medical Corporation. The device information was last updated on February 06, 2025.

This page provides complete registration details including device class (A5800), classification (Ligament and tendon surgery instrument / 靭帯・腱手術用器械), 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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PMDA Official Data
Bilingual (EN/JP)
MD
A5800
100812_28B3X10030SNA010_A_01_01
MD
A5800
引きドリルII用ガイド
引きドリルII用ガイド
PMDA ID: 100812_28B3X10030SNA010_A_01_01
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Device Classification / 分類
Device Type
MD
Device Class
A5800
Class Name (English)
Ligament and tendon surgery instrument
Class Name (日本語)
靭帯・腱手術用器械
Registration Information / 登録情報
PMDA ID
100812_28B3X10030SNA010_A_01_01
Last Update Date
February 06, 2025
Official Documents
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
Product Names / 製品名
Market Name (English)
引きドリルII用ガイド
Market Name (日本語)
引きドリルII用ガイド