Taiwan FDA registration 3ae5452dab94f4afbc2b29540ba9acca
“JO” PCF Posterior Cervical Fixation System
TW: “傑奎”比希弗頸椎後方固定系統
Taiwan·Risk Class 3·MD·Jiekui Technology Co., Ltd. Nanke Branch·Registered Sep 22, 2016 – Sep 22, 2026ActiveRegistration details
- Analysis ID
- 3ae5452dab94f4afbc2b29540ba9acca
- License Form
- Ministry of Health Medical Device Manufacturing No. 005453
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)
- N3070 Pedicle screw system
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 22, 2016
- Expiry Date
- Sep 22, 2026
About this record
Access comprehensive regulatory information for “JO” PCF Posterior Cervical Fixation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3ae5452dab94f4afbc2b29540ba9acca 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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