Taiwan FDA registration a50aca60750997f0855424d3abea36b9
"Difu" Kerui hip femoral head
TW: “帝富”可瑞髖關節股骨頭
Taiwan·Risk Class 2·DEPUY INTERNATIONAL LTD.·Registered Dec 25, 2007 – Dec 25, 2012CancelledRegistration details
- Analysis ID
- a50aca60750997f0855424d3abea36b9
- Customs Code
- DHA00601851908
Company information
- Manufacturer
- DEPUY INTERNATIONAL LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch
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.3353 Semi-restricted Segment Joints of Metallic/Ceramic/Polymer-like Bone Cement or Non-Porous Coating Cement-free Cement-type Supplements
- Import Information
- import
Dates and status
- Registration Date
- Dec 25, 2007
- Expiry Date
- Dec 25, 2012
- Cancellation Date
- Sep 26, 2016
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Difu" Kerui hip femoral head in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a50aca60750997f0855424d3abea36b9 and manufactured by DEPUY INTERNATIONAL LTD.. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.
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