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“Centinel Spine” Prodisc-C VIVO Total Disc Replacement Device - Taiwan Registration 4a4cdade88b1fbe548256ffc8d5e76cd

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..

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.

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4a4cdade88b1fbe548256ffc8d5e76cd
Registration Details
Taiwan FDA Registration: 4a4cdade88b1fbe548256ffc8d5e76cd
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Device Details

“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
Risk Class 3
MD

Registration Details

4a4cdade88b1fbe548256ffc8d5e76cd

Ministry of Health Medical Device Import No. 033620

DHA05603362003

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedic devices

N9999 Other

Imported from abroad

Dates and Status

Apr 28, 2020

Apr 28, 2025