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NX Three - PMDA ID 202449_224ADBZX00285000_B_01_08

エヌ・エックス・スリー

Access comprehensive regulatory information for NX Three (エヌ・エックス・スリー) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 202449_224ADBZX00285000_B_01_08 and manufactured by Envista Japan K.K.. The device information was last updated on July 31, 2024.

This page provides complete registration details including device class (C0500), classification (Dental composite resin cement / 歯科用コンポジットレジンセメント), 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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MD
C0500
202449_224ADBZX00285000_B_01_08
MD
C0500
NX Three
エヌ・エックス・スリー
PMDA ID: 202449_224ADBZX00285000_B_01_08
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Device Classification / 分類
Device Type
MD
Device Class
C0500
Class Name (English)
Dental composite resin cement
Class Name (日本語)
歯科用コンポジットレジンセメント
Registration Information / 登録情報
PMDA ID
202449_224ADBZX00285000_B_01_08
Last Update Date
July 31, 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)
NX Three
Market Name (日本語)
エヌ・エックス・スリー