Taiwan FDA registration 67ea1a687aafb47dad47703f412621a6
"Stryker" tibial femur fixation system
TW: "史賽克" 脛股骨固定系統
Taiwan·Risk Class 2·STRYKER TRAUMA GMBH.·Registered Feb 06, 2006 – Feb 06, 2026ExpiredRegistration details
- Analysis ID
- 67ea1a687aafb47dad47703f412621a6
- Customs Code
- DHA00601392201
Company information
- Manufacturer
- STRYKER TRAUMA GMBH.
- Manufacturer Country
- Germany
- 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
- Import Information
- import
Dates and status
- Registration Date
- Feb 06, 2006
- Expiry Date
- Feb 06, 2026
About this record
Access comprehensive regulatory information for "Stryker" tibial femur 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 67ea1a687aafb47dad47703f412621a6 and manufactured by STRYKER TRAUMA GMBH.. 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