Taiwan FDA registration 88825baf0b13afe4054a833df82b92d8
Merex M2 posterior spinal fixation system
TW: 美瑞世 M2 脊椎後方固定系統
Taiwan·Risk Class 2·Jiekui Technology Co., Ltd. Nanke Branch·Registered Nov 13, 2003 – Nov 13, 2028ActiveRegistration details
- Analysis ID
- 88825baf0b13afe4054a833df82b92d8
- Customs Code
- DHY00500105002
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
- 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
- Nov 13, 2003
- Expiry Date
- Nov 13, 2028
About this record
Access comprehensive regulatory information for Merex M2 posterior spinal fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 88825baf0b13afe4054a833df82b92d8 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