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"Singular" magnetic resonance imaging instrument - Taiwan Registration 33a66808cfa985d36498053cafecbbba

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 33a66808cfa985d36498053cafecbbba and manufactured by GE HANGWEI MEDICAL SYSTEMS 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 Healthcare(Tianjin) Company Limited, XINAOMDT TECHNOLOGY CO., LTD., 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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33a66808cfa985d36498053cafecbbba
Registration Details
Taiwan FDA Registration: 33a66808cfa985d36498053cafecbbba
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Device Details

"Singular" magnetic resonance imaging instrument
TW: โ€œๅฅ‡็•ฐโ€็ฃๆŒฏ้€ ๅฝฑๅ„€
Risk Class 2
Cancelled

Registration Details

33a66808cfa985d36498053cafecbbba

DHA04200028700

Company Information

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". Chinese goods

Dates and Status

Oct 18, 2010

Oct 18, 2015

Apr 25, 2018

Cancellation Information

Logged out

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