"Singular" magnetic resonance imaging instrument
Taiwan·Risk Class 2·GE Healthcare(Tianjin) Company Limited·Registered Feb 21, 2012 – Feb 21, 2022Cancelled- Analysis ID
- 9efbba182b4e6960a52d947f6e89f663
- Customs Code
- DHA04200032801
- Manufacturer
- GE Healthcare(Tianjin) Company Limited
- 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.
- Registration Date
- Feb 21, 2012
- Expiry Date
- Feb 21, 2022
- Cancellation Date
- Apr 12, 2024
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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 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.