Taiwan FDA registration 568a363c67c33e1f94db6a118d1336be
"Stryker" Solis vertebral neck guard system (sterilization)
TW: “史賽克”梭利斯椎頸護架系統(滅菌)
Taiwan·Risk Class 2·STRYKER SPINE SAS·Registered Jan 03, 2012 – Jan 03, 2027ActiveRegistration details
- Analysis ID
- 568a363c67c33e1f94db6a118d1336be
- Customs Code
- DHA00602315200
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
- Jan 03, 2012
- Expiry Date
- Jan 03, 2027
About this record
Access comprehensive regulatory information for "Stryker" Solis vertebral neck guard 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 568a363c67c33e1f94db6a118d1336be 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. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices