Taiwan FDA registration 133090f2002f3684b97b77d0b9e1615e
"Total" posterior spinal fusion system
TW: “全合”脊椎後方固定系統
Taiwan·Risk Class 2·Quanhe Biomedical Technology Co., Ltd·Registered Feb 16, 2007 – Feb 16, 2027ActiveRegistration details
- Analysis ID
- 133090f2002f3684b97b77d0b9e1615e
- Customs Code
- DHY00500213209
Company information
- Manufacturer
- Quanhe Biomedical Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- AAXTER 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.3070 椎弓螺釘系統
- Import Information
- Domestic
Dates and status
- Registration Date
- Feb 16, 2007
- Expiry Date
- Feb 16, 2027
About this record
Access comprehensive regulatory information for "Total" posterior spinal fusion system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 133090f2002f3684b97b77d0b9e1615e and manufactured by Quanhe Biomedical Technology Co., Ltd. The authorized representative in Taiwan is AAXTER CO., LTD..
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