Taiwan FDA registration ee025d1b0c25bfc765b09cd0a6701f37
“JO” Inter-X Lumbar Fusion Cage
TW: “傑奎”穎特司腰椎融合器
Taiwan·Risk Class 2·MD·Jiekui Technology Co., Ltd. Nanke Branch·Registered Sep 05, 2016 – Sep 05, 2026ActiveRegistration details
- Analysis ID
- ee025d1b0c25bfc765b09cd0a6701f37
- License Form
- Ministry of Health Medical Device Manufacturing No. 005447
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 Orthopedic devices
- Product Type (Level 2)
- N3060 Spine correction fixation between vertebral bodies
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 05, 2016
- Expiry Date
- Sep 05, 2026
About this record
Access comprehensive regulatory information for “JO” Inter-X Lumbar Fusion Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ee025d1b0c25bfc765b09cd0a6701f37 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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