Taiwan FDA registration 57bbdad4e8957e475d588984625284b8
"Stryker" Riffiths zero-notch cervical preneuravia fixation system
TW: “史賽克”芮菲斯零切跡頸椎前置骨板固定系統
Taiwan·Risk Class 2·STRYKER SPINE SAS·Registered Jun 08, 2010 – Jun 08, 2025ExpiredRegistration details
- Analysis ID
- 57bbdad4e8957e475d588984625284b8
- Customs Code
- DHA00602108804
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
- Jun 08, 2010
- Expiry Date
- Jun 08, 2025
About this record
Access comprehensive regulatory information for "Stryker" Riffiths zero-notch cervical preneuravia fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 57bbdad4e8957e475d588984625284b8 and manufactured by STRYKER SPINE SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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