Taiwan FDA registration 227ff95c7c02569fa797a248a0f480b0
“Centinel Spine” Prodisc-L Total Disc Replacement Device
TW: “伸特耐-脊椎”波帝斯人工腰椎椎間盤
Taiwan·Risk Class 3·MD·Centinel Spine, LLC·Registered Oct 21, 2021 – Oct 21, 2026ActiveRegistration details
- Analysis ID
- 227ff95c7c02569fa797a248a0f480b0
- License Form
- Ministry of Health Medical Device Import No. 034977
- Customs Code
- DHA05603497700
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 Orthopedic devices
- Product Type (Level 2)
- N9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 21, 2021
- Expiry Date
- Oct 21, 2026
About this record
Access comprehensive regulatory information for “Centinel Spine” Prodisc-L 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 227ff95c7c02569fa797a248a0f480b0 and manufactured by Centinel Spine, LLC. The authorized representative in Taiwan is RACK MEDICAL TECHNOLOGIES, INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices