Taiwan FDA registration cbe9962cfda85b8ee40c235ce1472a8c
“Centinel Spine” STALIF C
TW: “伸特耐-脊椎”司特立頸椎椎間融合器
Taiwan·Risk Class 2·MD·Centinel Spine, Inc.·Registered May 21, 2019 – May 21, 2024ExpiredRegistration details
- Analysis ID
- cbe9962cfda85b8ee40c235ce1472a8c
- License Form
- Ministry of Health Medical Device Import No. 032550
- Customs Code
- DHA05603255003
Company information
- Manufacturer
- Centinel Spine, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- RACK MEDICAL TECHNOLOGIES, INC.
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)
- N3060 Spine correction fixation between vertebral bodies
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 21, 2019
- Expiry Date
- May 21, 2024
About this record
Access comprehensive regulatory information for “Centinel Spine” STALIF C in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cbe9962cfda85b8ee40c235ce1472a8c and manufactured by Centinel Spine, Inc.. The authorized representative in Taiwan is RACK MEDICAL TECHNOLOGIES, INC..
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