Taiwan FDA registration e910339ac9c08783114d699b8c252463
“TEKNIMED” COHESION BONE CEMENT
TW: “泰克美”克西鈞脊固骨水泥
Taiwan·Risk Class 2·MD·Teknimed SAS·Registered Nov 26, 2013 – Nov 26, 2023CancelledRegistration details
- Analysis ID
- e910339ac9c08783114d699b8c252463
- License Form
- Ministry of Health Medical Device Import No. 025611
- Customs Code
- DHA05602561106
Company information
- Manufacturer
- Teknimed SAS
- Manufacturer Country
- France
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- 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
- Nov 26, 2013
- Expiry Date
- Nov 26, 2023
- Cancellation Date
- Aug 28, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “TEKNIMED” COHESION 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 e910339ac9c08783114d699b8c252463 and manufactured by Teknimed SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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