Taiwan FDA registration aa7df8aa740f207f2be23c744e9b4369
"Singular" patient information system
TW: "奇異"病患資訊系統
Taiwan·Risk Class 2·GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES·Registered Mar 23, 2006 – Mar 23, 2016CancelledRegistration details
- Analysis ID
- aa7df8aa740f207f2be23c744e9b4369
- Customs Code
- DHA00601419807
Company information
- Manufacturer
- GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
- Manufacturer Country
- United States
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Mar 23, 2006
- Expiry Date
- Mar 23, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Singular" patient information system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa7df8aa740f207f2be23c744e9b4369 and manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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