Taiwan FDA registration c455a6c6825e1dcad4e8a44901c56172
“Centinel Spine” MIDLINE II-TI
TW: “伸特耐-脊椎”美特耐腰椎椎間融合器
Taiwan·Risk Class 2·MD·Centinel Spine, LLC·Registered Nov 28, 2021 – Nov 28, 2026ActiveRegistration details
- Analysis ID
- c455a6c6825e1dcad4e8a44901c56172
- License Form
- Ministry of Health Medical Device Import No. 035070
- Customs Code
- DHA05603507004
Company information
- Manufacturer
- Centinel Spine, LLC
- Manufacturer Country
- United States
- Authorized Representative
- RACK MEDICAL TECHNOLOGIES, INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 28, 2021
- Expiry Date
- Nov 28, 2026
About this record
Access comprehensive regulatory information for “Centinel Spine” MIDLINE II-TI in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c455a6c6825e1dcad4e8a44901c56172 and manufactured by Centinel Spine, LLC. The authorized representative in Taiwan is RACK MEDICAL TECHNOLOGIES, INC..
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