Taiwan FDA registration b64529f3003e6acdf76bbbf71c0fb343
"Tekmei" European ridge replaces radiopaque bone cement
TW: “泰克美”歐配脊替不透射線骨水泥
Taiwan·Risk Class 2·TEKNIMED SAS·Registered Dec 27, 2014 – Dec 27, 2029ActiveRegistration details
- Analysis ID
- b64529f3003e6acdf76bbbf71c0fb343
- Customs Code
- DHA05602688802
Company information
- Manufacturer
- TEKNIMED SAS
- Manufacturer Country
- France
- Authorized Representative
- GREAT UNITED STRONG ENTERPRISE CO., LTD.
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.3027 PMMA骨水泥
- Import Information
- import
Dates and status
- Registration Date
- Dec 27, 2014
- Expiry Date
- Dec 27, 2029
About this record
Access comprehensive regulatory information for "Tekmei" European ridge replaces 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 b64529f3003e6acdf76bbbf71c0fb343 and manufactured by TEKNIMED SAS. The authorized representative in Taiwan is GREAT UNITED STRONG ENTERPRISE CO., LTD..
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