Taiwan FDA registration df0cc6843eb0519c24ee16f4581ff57c
"Schpaweis" lumbar intervertebral fusion device
TW: “施百威”腰椎椎間融合器
Taiwan·Risk Class 2·SPINEWAY Ltd·Registered Oct 30, 2010 – Oct 30, 2025ExpiredRegistration details
- Analysis ID
- df0cc6843eb0519c24ee16f4581ff57c
- Customs Code
- DHA00602161807
Company information
- Manufacturer
- SPINEWAY Ltd
- Manufacturer Country
- France
- Authorized Representative
- SUMMIT BIOMED. CO., LTD.
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.3060 椎體間之脊椎矯正固定物
- Import Information
- import
Dates and status
- Registration Date
- Oct 30, 2010
- Expiry Date
- Oct 30, 2025
About this record
Access comprehensive regulatory information for "Schpaweis" lumbar intervertebral fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df0cc6843eb0519c24ee16f4581ff57c and manufactured by SPINEWAY Ltd. The authorized representative in Taiwan is SUMMIT BIOMED. CO., LTD..
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