Taiwan FDA registration f7daf8b957443e410c4a71eabdd55c43
Stryker Manual Orthopedic Instruments (Sterilization)
TW: “史賽克”手動式骨科手術器械 (滅菌)
Taiwan·Risk Class 1·STRYKER TRAUMA GMBH.·Registered Sep 24, 2008 – Sep 24, 2018CancelledRegistration details
- Analysis ID
- f7daf8b957443e410c4a71eabdd55c43
- Customs Code
- DHA04400709207
Company information
- Manufacturer
- STRYKER TRAUMA GMBH.
- Manufacturer Country
- Germany
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Sep 24, 2008
- Expiry Date
- Sep 24, 2018
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Stryker Manual Orthopedic Instruments (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f7daf8b957443e410c4a71eabdd55c43 and manufactured by STRYKER TRAUMA GMBH.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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