Taiwan FDA registration 8bc999bbbd41b9f4768539b9fbacb5fa
Jacquie polymer cervical intervertebral fusion device
TW: 傑奎高分子頸椎椎間融合器
Taiwan·Risk Class 2·Jiekui Technology Co., Ltd. Nanke Branch·Registered Jan 16, 2012 – Jan 16, 2027ActiveRegistration details
- Analysis ID
- 8bc999bbbd41b9f4768539b9fbacb5fa
- Customs Code
- DHY00500357002
Company information
- Manufacturer
- Jiekui Technology Co., Ltd. Nanke Branch
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Jiekui Technology Co., Ltd. Nanke Branch
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
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Jan 16, 2012
- Expiry Date
- Jan 16, 2027
About this record
Access comprehensive regulatory information for Jacquie polymer cervical intervertebral fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8bc999bbbd41b9f4768539b9fbacb5fa and manufactured by Jiekui Technology Co., Ltd. Nanke Branch. The authorized representative in Taiwan is Jiekui Technology Co., Ltd. Nanke Branch.
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