Taiwan FDA registration 238f60cfe7cdb0de774d755cf67d4c19
"Spite" Romeo posterior lumbar fusion system
TW: “司佰特”羅密歐腰椎後路融合系統
Taiwan·Risk Class 2·SPINEART SA·Registered Dec 22, 2011 – Dec 22, 2026ActiveRegistration details
- Analysis ID
- 238f60cfe7cdb0de774d755cf67d4c19
- Customs Code
- DHA00602313602
Company information
- Manufacturer
- SPINEART SA
- Manufacturer Country
- Switzerland
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
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
- import
Dates and status
- Registration Date
- Dec 22, 2011
- Expiry Date
- Dec 22, 2026
About this record
Access comprehensive regulatory information for "Spite" Romeo posterior lumbar 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 238f60cfe7cdb0de774d755cf67d4c19 and manufactured by SPINEART SA. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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