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“Zimmer” NexGen Complete Knee Solution Augments - Taiwan Registration c1bc35478ad5b50147c63092492978ef

Access comprehensive regulatory information for “Zimmer” NexGen Complete Knee Solution Augments in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c1bc35478ad5b50147c63092492978ef and manufactured by ZIMMER, INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..

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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c1bc35478ad5b50147c63092492978ef
Registration Details
Taiwan FDA Registration: c1bc35478ad5b50147c63092492978ef
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Device Details

“Zimmer” NexGen Complete Knee Solution Augments
TW: “捷邁”新世紀人工膝關節墊塊
Risk Class 2
MD

Registration Details

c1bc35478ad5b50147c63092492978ef

Ministry of Health Medical Device Import No. 032865

DHA05603286502

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

Oct 10, 2019

Oct 10, 2024