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“Centinel Spine” Prodisc-L Total Disc Replacement Device - Taiwan Registration 227ff95c7c02569fa797a248a0f480b0

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..

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227ff95c7c02569fa797a248a0f480b0
Registration Details
Taiwan FDA Registration: 227ff95c7c02569fa797a248a0f480b0
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Device Details

“Centinel Spine” Prodisc-L Total Disc Replacement Device
TW: “伸特耐-脊椎”波帝斯人工腰椎椎間盤
Risk Class 3
MD

Registration Details

227ff95c7c02569fa797a248a0f480b0

Ministry of Health Medical Device Import No. 034977

DHA05603497700

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedic devices

N9999 Other

Imported from abroad

Dates and Status

Oct 21, 2021

Oct 21, 2026