Taiwan FDA registration beffeda25584f299c7a6299d32939474
"Stryker" Zedent acetabular cup system
TW: "史賽克"采登特髖臼杯系統
Taiwan·Risk Class 2·STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.·Registered May 07, 2003 – May 07, 2028ActiveRegistration details
- Analysis ID
- beffeda25584f299c7a6299d32939474
- Customs Code
- DHA00601029307
Company information
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- 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
- Contract manufacturing;; input
Dates and status
- Registration Date
- May 07, 2003
- Expiry Date
- May 07, 2028
About this record
Access comprehensive regulatory information for "Stryker" Zedent acetabular cup system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number beffeda25584f299c7a6299d32939474 and manufactured by STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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