"Stryker" cervical artificial disc
Taiwan·Risk Class 2·STRYKER SPINE SAS·Registered Mar 04, 2011 – Mar 04, 2016Cancelled- Analysis ID
- b5fb1726704eae58450dada5002fd451
- Customs Code
- DHA00602180009
- Manufacturer
- STRYKER SPINE SAS
- Manufacturer Country
- France
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
- Intended Use
- This product is indicated for the treatment of cervical radiculoradiculus symptoms (upper extremity pain and/or nerve damage) caused by loss of disc height, complications of disc/osteophytes, or single-level disc herniation between Neck 3 and Neck 7. This product is suitable for replacing a single-segment intervertebral disc between Neck 3 and Neck 7, increasing and maintaining the height of the intervertebral disc, relieving the terminal symptoms of the upper limbs, and improving the function of the treated vertebral segment to enable it to rotate.
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
- Registration Date
- Mar 04, 2011
- Expiry Date
- Mar 04, 2016
- Cancellation Date
- Apr 25, 2018
- Status
- Logged out
- Reason
- 自行鍵入
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Access comprehensive regulatory information for "Stryker" cervical artificial disc in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b5fb1726704eae58450dada5002fd451 and manufactured by STRYKER SPINE SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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