Taiwan FDA registration e32539e9aee714bef7954c889bf4458f
"Stryker" posterior open lumbar brasion system (sterilization)
TW: “史賽克”後開腰椎護架系統(滅菌)
Taiwan·Risk Class 2·STRYKER SPINE SAS·Registered Oct 17, 2012 – Oct 17, 2027ActiveRegistration details
- Analysis ID
- e32539e9aee714bef7954c889bf4458f
- Customs Code
- DHA00602406102
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
- Oct 17, 2012
- Expiry Date
- Oct 17, 2027
About this record
Access comprehensive regulatory information for "Stryker" posterior open lumbar brasion system (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e32539e9aee714bef7954c889bf4458f and manufactured by STRYKER SPINE SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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