Taiwan FDA registration 3fcf661fb073ffce621b26f5c50df14f
Forever Pure Danny Brown Splint (Unsterilized)
TW: 永純丹尼布朗夾板 (未滅菌)
Taiwan·Risk Class 1·Yongchun Prosthetic Co., Ltd. Tainan Factory·Registered Jan 05, 2006 – Jan 05, 2026ExpiredRegistration details
- Analysis ID
- 3fcf661fb073ffce621b26f5c50df14f
- Customs Code
- DHY04300092808
Company information
- Manufacturer
- Yongchun Prosthetic Co., Ltd. Tainan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- YONG CHWEN PROSTHETIC & ORTHOPEDIC INC.
Product details
- Intended Use
- Equipment used to immobilize the foot for medical purposes.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3675 丹尼布朗夾板
- Import Information
- Domestic
Dates and status
- Registration Date
- Jan 05, 2006
- Expiry Date
- Jan 05, 2026
About this record
Access comprehensive regulatory information for Forever Pure Danny Brown Splint (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3fcf661fb073ffce621b26f5c50df14f and manufactured by Yongchun Prosthetic Co., Ltd. Tainan Factory. The authorized representative in Taiwan is YONG CHWEN PROSTHETIC & ORTHOPEDIC INC..
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