Taiwan FDA registration fabe564398dfb1aa22c6ddfcf10a09bf
"Holly" PEEK intervertebral stent system
TW: “全合”聚醚醚酮椎間支架系統
Taiwan·Risk Class 2·Quanhe Biomedical Technology Co., Ltd·Registered Aug 20, 2012 – Aug 20, 2027ActiveRegistration details
- Analysis ID
- fabe564398dfb1aa22c6ddfcf10a09bf
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.3060 椎體間之脊椎矯正固定物
- Import Information
- Domestic
Dates and status
- Registration Date
- Aug 20, 2012
- Expiry Date
- Aug 20, 2027
About this record
Access comprehensive regulatory information for "Holly" PEEK intervertebral stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fabe564398dfb1aa22c6ddfcf10a09bf and manufactured by Quanhe Biomedical Technology Co., Ltd. The authorized representative in Taiwan is AAXTER CO., LTD..
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