Taiwan FDA registration c9000eda2c2f03a124b86f113435316d
"Singular" clinical information integration system
TW: “奇異”臨床資訊整合系統
Taiwan·Risk Class 2·GE HEALTHCARE FINLAND OY·Registered Jun 29, 2007 – Jun 29, 2017CancelledRegistration details
- Analysis ID
- c9000eda2c2f03a124b86f113435316d
- Customs Code
- DHA00601814901
Company information
- Manufacturer
- GE HEALTHCARE FINLAND OY
- Manufacturer Country
- Finland
- 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
- Product Type (Level 2)
- E.2300 Cardiac monitor (including cardiac data and heart rate monitor)
- Import Information
- import
Dates and status
- Registration Date
- Jun 29, 2007
- Expiry Date
- Jun 29, 2017
- Cancellation Date
- Nov 18, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Singular" clinical information integration system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c9000eda2c2f03a124b86f113435316d and manufactured by GE HEALTHCARE FINLAND OY. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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