Taiwan FDA registration 025dc62dbedd7be16155a88e62165df5
"Goodeka Osterning" Zedent acetabular component system
TW: “好美得卡 奧斯得寧”采登特髖臼組件系統
Taiwan·Risk Class 2·HOWMEDICA OSTEONICS CORP.·Registered Sep 02, 2011 – Sep 02, 2026ActiveRegistration details
- Analysis ID
- 025dc62dbedd7be16155a88e62165df5
- Customs Code
- DHA00602277107
Company information
- Manufacturer
- HOWMEDICA OSTEONICS CORP.
- Manufacturer Country
- United States
- 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 02, 2011
- Expiry Date
- Sep 02, 2026
About this record
Access comprehensive regulatory information for "Goodeka Osterning" Zedent acetabular component system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 025dc62dbedd7be16155a88e62165df5 and manufactured by HOWMEDICA OSTEONICS CORP.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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