Taiwan FDA registration acb03aeb7403f05d7c5916d2e873234c
"Singular" dual-frequency index and EEG monitoring module
TW: "奇異" 雙頻指數及腦電圖監測模組
Taiwan·Risk Class 2·GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES·Registered Oct 03, 2005 – Oct 03, 2015CancelledRegistration details
- Analysis ID
- acb03aeb7403f05d7c5916d2e873234c
- Customs Code
- DHA00601258201
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)
- K Neuroscience
- Product Type (Level 2)
- K.1400 Brain Wave Scanner
- Import Information
- import
Dates and status
- Registration Date
- Oct 03, 2005
- Expiry Date
- Oct 03, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Singular" dual-frequency index and EEG monitoring module in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number acb03aeb7403f05d7c5916d2e873234c and manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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