Pure Global

X-Guide Components - PMDA ID 202449_13B1X10405400064_A_01_02

X−ガイド コンポーネント

Access comprehensive regulatory information for X-Guide Components (X−ガイド コンポーネント) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 202449_13B1X10405400064_A_01_02 and manufactured by Envista Japan K.K.. The device information was last updated on June 07, 2024.

This page provides complete registration details including device class (A5800), classification (Bone surgery instrument / 骨手術用器械), 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 Database
Powered by Pure Global AI
PMDA Official Data
Bilingual (EN/JP)
MD
A5800
202449_13B1X10405400064_A_01_02
MD
A5800
X-Guide Components
X−ガイド コンポーネント
PMDA ID: 202449_13B1X10405400064_A_01_02
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification / 分類
Device Type
MD
Device Class
A5800
Class Name (English)
Bone surgery instrument
Class Name (日本語)
骨手術用器械
Registration Information / 登録情報
PMDA ID
202449_13B1X10405400064_A_01_02
Last Update Date
June 07, 2024
Official Documents
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/エンビスタジャパン株式会社
Product Names / 製品名
Market Name (English)
X-Guide Components
Market Name (日本語)
X−ガイド コンポーネント