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“Zimmer” NexGen Prolong Highly Crosslinked Polyethylene Inset All Poly Patella - Taiwan Registration 27cf5e1da9294cf767d8cfd83f08c57a

Access comprehensive regulatory information for “Zimmer” NexGen Prolong Highly Crosslinked Polyethylene Inset All Poly Patella in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 27cf5e1da9294cf767d8cfd83f08c57a and manufactured by ZIMMER,INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..

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27cf5e1da9294cf767d8cfd83f08c57a
Registration Details
Taiwan FDA Registration: 27cf5e1da9294cf767d8cfd83f08c57a
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Device Details

“Zimmer” NexGen Prolong Highly Crosslinked Polyethylene Inset All Poly Patella
TW: “捷邁”新世紀高分子聚乙烯人工膝關節用髕骨
Risk Class 2
MD

Registration Details

27cf5e1da9294cf767d8cfd83f08c57a

Ministry of Health Medical Device Import No. 025742

DHA05602574208

Company Information

United States

Product Details

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

N Orthopedic devices

N3560 Semi-restrictive knee femoral tibial polymer/metal/polymeric cement compound

Imported from abroad

Dates and Status

Dec 25, 2013

Dec 25, 2028