Taiwan FDA registration 22bc987393f60bb87ae5176506bfa84f
"Jacqui" carbon fiber polymer composite lumbar fusion device
TW: “傑奎”碳纖維高分子複材腰椎融合器
Taiwan·Risk Class 2·Jiekui Technology Co., Ltd. Nanke Branch·Registered Aug 31, 2012 – Aug 31, 2027ActiveRegistration details
- Analysis ID
- 22bc987393f60bb87ae5176506bfa84f
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
- Aug 31, 2012
- Expiry Date
- Aug 31, 2027
About this record
Access comprehensive regulatory information for "Jacqui" carbon fiber polymer composite lumbar 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 22bc987393f60bb87ae5176506bfa84f 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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