Taiwan FDA registration 9d8d119f7c4fa68be4229525fda81ccc
"Jacquie" polymer lumbar intervertebral fusion device
TW: “傑奎”高分子腰椎椎間融合器
Taiwan·Risk Class 2·Jiekui Technology Co., Ltd. Nanke Branch·Registered Apr 17, 2012 – Apr 17, 2027ActiveRegistration details
- Analysis ID
- 9d8d119f7c4fa68be4229525fda81ccc
- Customs Code
- DHY00500363501
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
- Apr 17, 2012
- Expiry Date
- Apr 17, 2027
About this record
Access comprehensive regulatory information for "Jacquie" polymer lumbar 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 9d8d119f7c4fa68be4229525fda81ccc 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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