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"Fujifilm Film" MRI imaging device - Taiwan Registration 82949facd2885e50607b836d08def1bd

Access comprehensive regulatory information for "Fujifilm Film" MRI imaging device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 82949facd2885e50607b836d08def1bd 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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82949facd2885e50607b836d08def1bd
Registration Details
Taiwan FDA Registration: 82949facd2885e50607b836d08def1bd
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Device Details

"Fujifilm Film" MRI imaging device
TW: โ€œๅฏŒๅฃซ่ปŸ็‰‡โ€ๆ ธ็ฃๅ…ฑๆŒฏๅฝฑๅƒ่ฃ็ฝฎ
Risk Class 2

Registration Details

82949facd2885e50607b836d08def1bd

DHA00601066100

Product Details

P Radiology Science

import

Dates and Status

May 21, 2004

May 21, 2029