"Singular" magnetic resonance imaging instrument
- Analysis ID
- 931b9f6938cf406ae4dc663b73e997fd
- Customs Code
- DHA04200032403
- Manufacturer
- XINAOMDT TECHNOLOGY 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
- 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
- Registration Date
- Jan 09, 2012
- Expiry Date
- Jan 09, 2017
- Cancellation Date
- Nov 18, 2019
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 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.