Taiwan FDA registration 514c1734e9b85715bac31edfb2557559
"Stryker" total artificial knee system
TW: "史賽克"全人工膝關節系統
Taiwan·Risk Class 2·STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.·Registered May 23, 2002 – May 23, 2022CancelledRegistration details
- Analysis ID
- 514c1734e9b85715bac31edfb2557559
- Customs Code
- DHA00600993100
Company information
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- May 23, 2002
- Expiry Date
- May 23, 2022
- Cancellation Date
- Jun 20, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Stryker" total 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 514c1734e9b85715bac31edfb2557559 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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