Taiwan FDA registration 4680ac8893a063f760f991b3a77d93e2
"Holly" polyetheretherketone anterior cervical intervertebral fusion
TW: “全合”聚醚醚酮前方頸椎椎間融合器
Taiwan·Risk Class 2·Quanhe Biomedical Technology Co., Ltd·Registered Dec 08, 2009 – Dec 08, 2029ActiveRegistration details
- Analysis ID
- 4680ac8893a063f760f991b3a77d93e2
- Customs Code
- DHY00500285000
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
- Dec 08, 2009
- Expiry Date
- Dec 08, 2029
About this record
Access comprehensive regulatory information for "Holly" polyetheretherketone anterior cervical intervertebral fusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4680ac8893a063f760f991b3a77d93e2 and manufactured by Quanhe Biomedical Technology Co., Ltd. The authorized representative in Taiwan is AAXTER CO., LTD..
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