Taiwan FDA registration 4a4cdade88b1fbe548256ffc8d5e76cd
“Centinel Spine” Prodisc-C VIVO Total Disc Replacement Device
TW: “伸特耐-脊椎”波帝斯人工頸椎椎間盤
Taiwan·Risk Class 3·MD·Centinel Spine, Inc.·Registered Apr 28, 2020 – Apr 28, 2025ExpiredRegistration details
- Analysis ID
- 4a4cdade88b1fbe548256ffc8d5e76cd
- License Form
- Ministry of Health Medical Device Import No. 033620
- Customs Code
- DHA05603362003
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)
- N9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 28, 2020
- Expiry Date
- Apr 28, 2025
About this record
Access comprehensive regulatory information for “Centinel Spine” Prodisc-C VIVO Total Disc Replacement Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4a4cdade88b1fbe548256ffc8d5e76cd and manufactured by Centinel Spine, Inc.. The authorized representative in Taiwan is RACK MEDICAL TECHNOLOGIES, INC..
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