Taiwan FDA registration cfa9ef49db748f79e3eeca233174d3c2
“Teknimed” OsseoFix+ Radiopaque Bone Cement
TW: “泰科妮美”歐瑟菲斯骨水泥
Taiwan·Risk Class 2·MD·TEKNIMED SAS·Registered Dec 30, 2014 – Dec 30, 2024ExpiredRegistration details
- Analysis ID
- cfa9ef49db748f79e3eeca233174d3c2
- License Form
- Ministry of Health Medical Device Import No. 026894
- Customs Code
- DHA05602689400
Company information
- Manufacturer
- TEKNIMED SAS
- Manufacturer Country
- France
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3027 PMMA bone cement
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 30, 2014
- Expiry Date
- Dec 30, 2024
About this record
Access comprehensive regulatory information for “Teknimed” OsseoFix+ Radiopaque Bone Cement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cfa9ef49db748f79e3eeca233174d3c2 and manufactured by TEKNIMED SAS. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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