Taiwan FDA registration 8e0ff955ea1625b942644fb2931b0620
“Synthes” TRAUMACEM V+ Bone Cement, Injectable
TW: “信迪思”骨科增強用骨水泥
Taiwan·Risk Class 2·MD·SYNTHES GMBH·Registered Nov 06, 2018 – Nov 06, 2028ActiveRegistration details
- Analysis ID
- 8e0ff955ea1625b942644fb2931b0620
- License Form
- Ministry of Health Medical Device Import No. 031712
- Customs Code
- DHA05603171201
Company information
- Manufacturer
- SYNTHES GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN 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
- Nov 06, 2018
- Expiry Date
- Nov 06, 2028
About this record
Access comprehensive regulatory information for “Synthes” TRAUMACEM V+ Bone Cement, Injectable in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8e0ff955ea1625b942644fb2931b0620 and manufactured by SYNTHES GMBH. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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