Taiwan FDA registration 3765484652067878cfea493b723a9481
"Stryker" Epigi artificial hip joint
TW: "史賽克"愛必吉人工髖關節
Taiwan·Risk Class 2·STRYKER IRELAND LIMITED·Registered Sep 11, 2006 – Sep 11, 2021CancelledRegistration details
- Analysis ID
- 3765484652067878cfea493b723a9481
- Customs Code
- DHA00601710107
Company information
- Manufacturer
- STRYKER IRELAND LIMITED
- Manufacturer Country
- Ireland
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
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
- Sep 11, 2006
- Expiry Date
- Sep 11, 2021
- Cancellation Date
- Sep 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Stryker" Epigi artificial hip joint in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3765484652067878cfea493b723a9481 and manufactured by STRYKER IRELAND LIMITED. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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