Taiwan FDA registration b483f1ea334a0a641b968b0778ddc9f0

"Fujifilm Film" magnetic resonance imaging system

TW: “富士軟片”磁振造影系統

Taiwan·Risk Class 2·FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa·Registered Apr 14, 2021 – Apr 14, 2026Expired

Registration details

Analysis ID: b483f1ea334a0a641b968b0778ddc9f0
Customs Code: DHA05603449801

Company information

Manufacturer: FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa
Manufacturer Country: Japan
Authorized Representative: FUJIFILM HEALTHCARE TAIWAN CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): P Radiology Science
Product Type (Level 2): P.1000 磁振診斷裝置
Import Information: Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and status

Registration Date: Apr 14, 2021
Expiry Date: Apr 14, 2026

About this record

Access comprehensive regulatory information for "Fujifilm Film" magnetic resonance imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b483f1ea334a0a641b968b0778ddc9f0 and manufactured by FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.