Taiwan FDA registration 4b8b67e97bf5ba38164f3f376bf205b6
"Goodeka Osdenin" Skobio classic all-artificial knee system
TW: “好美得卡-奧斯得寧”斯高比歐經典全人工膝關節系統
Registration details
- Analysis ID
- 4b8b67e97bf5ba38164f3f376bf205b6
- Customs Code
- DHA00602237601
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.3565 Knee jointsFemoral metals/polymersPorous coatings of cementless cement
- Import Information
- import
Dates and status
- Registration Date
- May 09, 2011
- Expiry Date
- May 09, 2021
- Cancellation Date
- Aug 17, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Goodeka Osdenin" Skobio classic all-artificial knee system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b8b67e97bf5ba38164f3f376bf205b6 and manufactured by HOWMEDICA OSTEONICS CORP.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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