Taiwan FDA registration e2e8c46efe3d4f83f8cf005baf0dfa1d
"Holly" polyetheretherketone lumbar intervertebral fusion
TW: “全合”聚醚醚酮腰椎椎間融合器
Taiwan·Risk Class 2·Quanhe Biomedical Technology Co., Ltd·Registered Apr 14, 2009 – Apr 14, 2029ActiveRegistration details
- Analysis ID
- e2e8c46efe3d4f83f8cf005baf0dfa1d
- Customs Code
- DHY00500268205
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
- Apr 14, 2009
- Expiry Date
- Apr 14, 2029
About this record
Access comprehensive regulatory information for "Holly" polyetheretherketone lumbar 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 e2e8c46efe3d4f83f8cf005baf0dfa1d and manufactured by Quanhe Biomedical Technology Co., Ltd. The authorized representative in Taiwan is AAXTER CO., LTD..
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