Taiwan FDA registration 5a82d438233c90056d7ebd0751c17b55
"Merits" Pushen II posterior spinal fixator
TW: “美瑞世”普生二代後方脊椎固定器
Taiwan·Risk Class 2·Jiekui Technology Co., Ltd. Nanke Branch·Registered Sep 02, 2009 – Sep 02, 2029ActiveRegistration details
- Analysis ID
- 5a82d438233c90056d7ebd0751c17b55
- Customs Code
- DHY00500277601
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.3070 椎弓螺釘系統
- Import Information
- Domestic
Dates and status
- Registration Date
- Sep 02, 2009
- Expiry Date
- Sep 02, 2029
About this record
Access comprehensive regulatory information for "Merits" Pushen II posterior spinal fixator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5a82d438233c90056d7ebd0751c17b55 and manufactured by Jiekui Technology Co., Ltd. Nanke Branch. The authorized representative in Taiwan is Jiekui Technology Co., Ltd. Nanke Branch.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices