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"Fujifilm Film" magnetic resonance imaging system - Taiwan Registration b483f1ea334a0a641b968b0778ddc9f0

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.

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b483f1ea334a0a641b968b0778ddc9f0
Registration Details
Taiwan FDA Registration: b483f1ea334a0a641b968b0778ddc9f0
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Device Details

"Fujifilm Film" magnetic resonance imaging system
TW: โ€œๅฏŒๅฃซ่ปŸ็‰‡โ€็ฃๆŒฏ้€ ๅฝฑ็ณป็ตฑ
Risk Class 2

Registration Details

b483f1ea334a0a641b968b0778ddc9f0

DHA05603449801

Product Details

For details, it is Chinese approved copy of the imitation order

P Radiology Science

P.1000 ็ฃๆŒฏ่จบๆ–ท่ฃ็ฝฎ

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

Apr 14, 2021

Apr 14, 2026