Taiwan FDA registration 3ac192a344ae2298e00566ff54c1e28f
Femur/condyle titanium alloy bone nail plate system
TW: 股骨/髁骨鈦合金骨釘骨板系統
Taiwan·STRYKER TRAUMA-SELZACH AG·Registered Jun 29, 1999 – Feb 09, 2004CancelledRegistration details
- Analysis ID
- 3ac192a344ae2298e00566ff54c1e28f
- Customs Code
- DHA00600922401
Company information
- Manufacturer
- STRYKER TRAUMA-SELZACH AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Product Type (Level 1)
- 0399 Other artificial function substitutes
- Import Information
- import
Dates and status
- Registration Date
- Jun 29, 1999
- Expiry Date
- Feb 09, 2004
- Cancellation Date
- Jul 18, 2007
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Femur/condyle titanium alloy bone nail plate system in Taiwan's medical device market through Pure Global AI's free database. is registered under number 3ac192a344ae2298e00566ff54c1e28f and manufactured by STRYKER TRAUMA-SELZACH AG. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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