Taiwan FDA registration 5181b348773ba1ea197bf21ea6eed4ee
"Dafoya" splint raw material (unsterilized)
TW: “達弗亞”夾板原料 (未滅菌)
Taiwan·Risk Class 1·WFR/AQUAPLAST CORPORATION·Registered Jan 22, 2009 – Jan 22, 2024CancelledRegistration details
- Analysis ID
- 5181b348773ba1ea197bf21ea6eed4ee
- Customs Code
- DHA04400742508
Company information
- Manufacturer
- WFR/AQUAPLAST CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- BOULDER ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Splints for Non-Expanded Limbs (I.3910)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3910 Clip board for non-bulging limbs
- Import Information
- import
Dates and status
- Registration Date
- Jan 22, 2009
- Expiry Date
- Jan 22, 2024
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Dafoya" splint raw material (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5181b348773ba1ea197bf21ea6eed4ee and manufactured by WFR/AQUAPLAST CORPORATION. The authorized representative in Taiwan is BOULDER ENTERPRISE CO., LTD..
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