Taiwan FDA registration 26bf793f1c511917a23c8ebe05acacff
“Teknimed” Cementek LV Synthetic Bone Substitute
TW: “泰克美”希曼骼低黏度人工替代骨
Taiwan·Risk Class 2·MD·TEKNIMED SAS·Registered Jan 28, 2016 – Jan 28, 2021CancelledRegistration details
- Analysis ID
- 26bf793f1c511917a23c8ebe05acacff
- License Form
- Ministry of Health Medical Device Import No. 028172
- Customs Code
- DHA05602817208
Company information
- Manufacturer
- TEKNIMED SAS
- Manufacturer Country
- France
- Authorized Representative
- GREAT UNITED STRONG ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3045 Resorbed calcium salt bone cavity filling device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 28, 2016
- Expiry Date
- Jan 28, 2021
- Cancellation Date
- Aug 28, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Teknimed” Cementek LV Synthetic Bone Substitute in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 26bf793f1c511917a23c8ebe05acacff and manufactured by TEKNIMED SAS. The authorized representative in Taiwan is GREAT UNITED STRONG ENTERPRISE CO., LTD..
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