Japan PMDA registration 340017_09B2X00010G00008_A_01_03

ジーシーインプラントRe・補綴用インスツルメント マシーン用スキルドライバーPlus

JP: ジーシーインプラントRe・補綴用インスツルメント マシーン用スキルドライバーPlus
Japan flagJapan·MD·A5803·Updated January 10, 2025
Device classification / 分類
Device Type
MD
Device Class
A5803
Class Name (English)
Surgical screwdriver
Class Name (日本語)
手術用ネジ回し
Registration information / 登録情報
PMDA ID
340017_09B2X00010G00008_A_01_03
Last Update Date
January 10, 2025
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/株式会社シオダ
About this record

Access comprehensive regulatory information for ジーシーインプラントRe・補綴用インスツルメント マシーン用スキルドライバーPlus (ジーシーインプラントRe・補綴用インスツルメント マシーン用スキルドライバーPlus) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 340017_09B2X00010G00008_A_01_03 and manufactured by Shioda Corporation. The device information was last updated on January 10, 2025.

This page provides complete registration details including device class (A5803), classification (Surgical screwdriver / 手術用ネジ回し), 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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