"Singular" magnetic resonance imaging instrument - Taiwan Registration 9efbba182b4e6960a52d947f6e89f663

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 9efbba182b4e6960a52d947f6e89f663 and manufactured by GE Healthcare(Tianjin) Company Limited. 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., 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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9efbba182b4e6960a52d947f6e89f663

Registration Details

Taiwan FDA Registration: 9efbba182b4e6960a52d947f6e89f663

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Device Details

"Singular" magnetic resonance imaging instrument

TW: “奇異”磁振造影儀

Risk Class 2

Cancelled

Registration Details

Analysis ID

9efbba182b4e6960a52d947f6e89f663

Customs Code

DHA04200032801

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

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.