Taiwan FDA registration 040f52541c446a8e05f5548d208811e9
"GE" Noninflatable extremity splint (Non-Sterile)
TW: "奇異" 非膨脹式四肢用夾板 (未滅菌)
Registration details
- Analysis ID
- 040f52541c446a8e05f5548d208811e9
- License Form
- Ministry of Health Medical Device Import Registration No. 012273
- Customs Code
- DHA08401227302
Company information
- Manufacturer
- GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
- Manufacturer Country
- United States
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, LTD.
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I3910 Splints for non-inflated extremities
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "GE" Noninflatable extremity splint (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 040f52541c446a8e05f5548d208811e9 and manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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