Taiwan FDA registration 24f0be874534a90012324c5e2ff5a677
"Singular" transcutaneous blood gas monitoring module
TW: "奇異" 經皮血液氣體監測模組
Taiwan·Risk Class 2·GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES·Registered Oct 04, 2005 – Oct 04, 2015CancelledRegistration details
- Analysis ID
- 24f0be874534a90012324c5e2ff5a677
- Customs Code
- DHA00601258708
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)
- D Anesthesiology
- Import Information
- import
Dates and status
- Registration Date
- Oct 04, 2005
- Expiry Date
- Oct 04, 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" transcutaneous blood gas 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 24f0be874534a90012324c5e2ff5a677 and manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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