Taiwan FDA registration af1f4e6fe79384d28c832df0e01f8b3a
"S & F" Robo splint (Non-Sterile)
TW: "艾斯恩富" 若玻樹脂石膏固定板 (未滅菌)
Taiwan·Risk Class 1·MD·S&F INC.·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- af1f4e6fe79384d28c832df0e01f8b3a
- License Form
- Ministry of Health Medical Device Import Registration No. 002387
- Customs Code
- DHA08400238701
Company information
- Manufacturer
- S&F INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- DURAMED INTERNATIONAL CORPORATION
Product details
- Intended Use
- Limb equipment is a medical device worn on the upper or lower limbs to support, correct or prevent deformation, and to straighten the body structure for functional improvement.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "S & F" Robo 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 af1f4e6fe79384d28c832df0e01f8b3a and manufactured by S&F INC.. The authorized representative in Taiwan is DURAMED INTERNATIONAL CORPORATION.
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