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“Zimmer” Allofit IT Alloclassic Acetabular Shell - Taiwan Registration 53a417df20680f870d53fee08cd4de8a

Access comprehensive regulatory information for “Zimmer” Allofit IT Alloclassic Acetabular Shell in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 53a417df20680f870d53fee08cd4de8a and manufactured by ZIMMER GMBH. 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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53a417df20680f870d53fee08cd4de8a
Registration Details
Taiwan FDA Registration: 53a417df20680f870d53fee08cd4de8a
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Device Details

“Zimmer” Allofit IT Alloclassic Acetabular Shell
TW: “捷邁”艾洛菲艾提人工髖臼杯
Risk Class 2
MD
Cancelled

Registration Details

53a417df20680f870d53fee08cd4de8a

Ministry of Health Medical Device Import No. 026778

DHA05602677808

Company Information

Switzerland

Product Details

N Orthopedic devices

N3350 Semi-restricted hip metal/polymer cement compound

Imported from abroad

Dates and Status

Nov 10, 2014

Nov 10, 2019

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者