Taiwan FDA registration 08193565d8085375c35de59c5620c2f7
"Siemens" whole body X-ray spiral computed tomography system
TW: "西門子" 全身X光螺旋電腦斷層掃描系統
Taiwan·Risk Class 2·SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.·Registered Mar 08, 2006 – Mar 08, 2021CancelledRegistration details
- Analysis ID
- 08193565d8085375c35de59c5620c2f7
- Customs Code
- DHAS4200009802
Company information
- Manufacturer
- SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.
- Manufacturer Country
- China
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Import Information
- Input;; Chinese goods;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
- Registration Date
- Mar 08, 2006
- Expiry Date
- Mar 08, 2021
- Cancellation Date
- Aug 04, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Siemens" whole body X-ray spiral computed tomography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 08193565d8085375c35de59c5620c2f7 and manufactured by SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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