Taiwan FDA registration 545fe4e01361d901984909a517fdc755
"Stryker" side-open lumbar fusion device (sterilization)
TW: “史賽克”側開腰椎間融合器(滅菌)
Taiwan·Risk Class 2·STRYKER SPINE SAS·Registered Mar 22, 2012 – Mar 22, 2027ActiveRegistration details
- Analysis ID
- 545fe4e01361d901984909a517fdc755
- Customs Code
- DHA00602338507
Company information
- Manufacturer
- STRYKER SPINE SAS
- Manufacturer Country
- France
- 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.3060 椎體間之脊椎矯正固定物
- Import Information
- import
Dates and status
- Registration Date
- Mar 22, 2012
- Expiry Date
- Mar 22, 2027
About this record
Access comprehensive regulatory information for "Stryker" side-open lumbar fusion device (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 545fe4e01361d901984909a517fdc755 and manufactured by STRYKER SPINE SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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