"Stryker" intervertebral fusion device
- Analysis ID
- aa8081e21bea3898d768fa20ea5cca11
- Customs Code
- DHA00601795602
- Manufacturer
- STRYKER SPINE SAS
- Manufacturer Country
- France
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
- Registration Date
- Mar 23, 2007
- Expiry Date
- Mar 23, 2027
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Access comprehensive regulatory information for "Stryker" intervertebral fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa8081e21bea3898d768fa20ea5cca11 and manufactured by STRYKER SPINE SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STRYKER SPINE SAS, and 2 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.