Taiwan FDA registration fe5fee65f588f53d8f364762788ba1b9
"Ximei" rotatable artificial femur repair system
TW: “西美”可旋式人工股骨修補系統
Taiwan·Risk Class 3·ZIMMER,INC.·Registered Oct 09, 2008 – Oct 09, 2028ActiveRegistration details
- Analysis ID
- fe5fee65f588f53d8f364762788ba1b9
- Customs Code
- DHA00601926702
Company information
- Manufacturer
- ZIMMER,INC.
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Zimmer Medical Device Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3330 Semi-restrictive hip metal/metal containing cemented acetabular assemblies as a supplement
- Import Information
- import
Dates and status
- Registration Date
- Oct 09, 2008
- Expiry Date
- Oct 09, 2028
About this record
Access comprehensive regulatory information for "Ximei" rotatable artificial femur repair system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number fe5fee65f588f53d8f364762788ba1b9 and manufactured by ZIMMER,INC.. The authorized representative in Taiwan is Taiwan Zimmer Medical Device Co., Ltd.
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