Taiwan FDA registration a687a6f76bc5c7a7be26ce4ddd311497
"Stryker" lumbar artificial disc
TW: “史賽克”腰椎人工椎間盤
Taiwan·Risk Class 3·STRYKER SPINE SAS·Registered Sep 17, 2008 – Sep 17, 2013CancelledRegistration details
- Analysis ID
- a687a6f76bc5c7a7be26ce4ddd311497
- Customs Code
- DHA00601944102
Company information
- Manufacturer
- STRYKER SPINE SAS
- Manufacturer Country
- France
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- Indicated for the treatment of lumbar discogenic pain associated with degenerative disc disease (DDD). Replacing a single lumbar disc (L1-S1) with degenerative disease allows flexibility in the portion to be treated, improves function, and reduces back pain associated with DDD.
- 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
- Sep 17, 2008
- Expiry Date
- Sep 17, 2013
- Cancellation Date
- Nov 15, 2016
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Stryker" lumbar artificial disc in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a687a6f76bc5c7a7be26ce4ddd311497 and manufactured by STRYKER SPINE SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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