"Singular" magnetic resonance imaging instrument
Taiwan·Risk Class 2·GE HANGWEI MEDICAL SYSTEMS CO. LTD.·Registered Oct 18, 2010 – Oct 18, 2015Cancelled- Analysis ID
- 33a66808cfa985d36498053cafecbbba
- Customs Code
- DHA04200028700
- Manufacturer
- GE HANGWEI MEDICAL SYSTEMS CO. LTD.
- Manufacturer Country
- China
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, LTD.
- 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". Chinese goods
- Registration Date
- Oct 18, 2010
- Expiry Date
- Oct 18, 2015
- Cancellation Date
- Apr 25, 2018
- Status
- Logged out
- Reason
- 自行鍵入
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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.