Taiwan FDA registration 931b9f6938cf406ae4dc663b73e997fd

"Singular" magnetic resonance imaging instrument

TW: “奇異”磁振造影儀
Taiwan flagTaiwan·Risk Class 2·XINAOMDT TECHNOLOGY CO., LTD.·Registered Jan 09, 2012 – Jan 09, 2017Cancelled
Registration details
Analysis ID
931b9f6938cf406ae4dc663b73e997fd
Customs Code
DHA04200032403
Company information
Manufacturer Country
China
Authorized Representative
GE MEDICAL SYSTEMS TAIWAN, 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
Chinese goods;; 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". input
Dates and status
Registration Date
Jan 09, 2012
Expiry Date
Jan 09, 2017
Cancellation Date
Nov 18, 2019
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Singular" magnetic resonance imaging instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 931b9f6938cf406ae4dc663b73e997fd and manufactured by XINAOMDT TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including GE HANGWEI MEDICAL SYSTEMS CO. LTD., GE Healthcare(Tianjin) Company Limited, and 2 recent registrations in the same category. 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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