Taiwan FDA registration b40e2259c8cf8231cba8f706aa3f4f70
“Syrison” Interbody Fusion System
TW: “喜瑞森”椎間融合系統
Taiwan·Risk Class 2·MD·Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory·Registered Oct 30, 2019 – Oct 30, 2024ExpiredRegistration details
- Analysis ID
- b40e2259c8cf8231cba8f706aa3f4f70
- License Form
- Ministry of Health Medical Device Manufacturing No. 006536
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WILTROM CO., LTD.
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)
- N3080 Interbody fusion device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 30, 2019
- Expiry Date
- Oct 30, 2024
About this record
Access comprehensive regulatory information for “Syrison” Interbody Fusion System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b40e2259c8cf8231cba8f706aa3f4f70 and manufactured by Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory. The authorized representative in Taiwan is WILTROM CO., LTD..
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