Pure Global

ultrasound imaging system EPIQ/Affiniti - PMDA ID 670277_225ADBZX00148000_B_01_18

超音波画像診断装置 EPIQ/Affiniti

Access comprehensive regulatory information for ultrasound imaging system EPIQ/Affiniti (超音波画像診断装置 EPIQ/Affiniti) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 670277_225ADBZX00148000_B_01_18 and manufactured by Philips Japan Inc.. The device information was last updated on January 14, 2025.

This page provides complete registration details including device class (A1200), classification (General-purpose ultrasound diagnostic imaging system / 汎用超音波画像診断装置), 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
A1200
670277_225ADBZX00148000_B_01_18
MD
A1200
ultrasound imaging system EPIQ/Affiniti
超音波画像診断装置 EPIQ/Affiniti
PMDA ID: 670277_225ADBZX00148000_B_01_18
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
A1200
Class Name (English)
General-purpose ultrasound diagnostic imaging system
Class Name (日本語)
汎用超音波画像診断装置
Registration Information / 登録情報
PMDA ID
670277_225ADBZX00148000_B_01_18
Last Update Date
January 14, 2025
Official Documents
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/株式会社フィリップス・ジャパン
Product Names / 製品名
Market Name (English)
ultrasound imaging system EPIQ/Affiniti
Market Name (日本語)
超音波画像診断装置 EPIQ/Affiniti