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"Singular" magnetic resonance imaging instrument - Taiwan Registration 931b9f6938cf406ae4dc663b73e997fd

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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931b9f6938cf406ae4dc663b73e997fd
Registration Details
Taiwan FDA Registration: 931b9f6938cf406ae4dc663b73e997fd
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Device Details

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

Registration Details

931b9f6938cf406ae4dc663b73e997fd

DHA04200032403

Company Information

Product Details

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

P Radiology Science

P.1000 ็ฃๆŒฏ่จบๆ–ท่ฃ็ฝฎ

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

Jan 09, 2012

Jan 09, 2017

Nov 18, 2019

Cancellation Information

Logged out

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