Taiwan FDA registration 81c74d77284801d185247299097eed6d
“WFR” Aquaplast Splinting Materials (Non-sterile)
TW: “達弗亞”夾板原料 (未滅菌)
Taiwan·Risk Class 1·MD·WFR/AQUAPLAST CORPORATION·Registered Oct 01, 2021 – Oct 31, 2024ExpiredRegistration details
- Analysis ID
- 81c74d77284801d185247299097eed6d
- License Form
- Ministry of Health Medical Device Import Registration No. 007425
- Customs Code
- DHA08400742505
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 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, 2024
About this record
Access comprehensive regulatory information for “WFR” Aquaplast Splinting Materials (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 81c74d77284801d185247299097eed6d and manufactured by WFR/AQUAPLAST CORPORATION. The authorized representative in Taiwan is BOULDER ENTERPRISE CO., LTD..
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