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"Zimmer" Longje Eti restricted liner - Taiwan Registration 49ab046ae437accb41d1f344be1181f6

Access comprehensive regulatory information for "Zimmer" Longje Eti restricted liner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49ab046ae437accb41d1f344be1181f6 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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49ab046ae437accb41d1f344be1181f6
Registration Details
Taiwan FDA Registration: 49ab046ae437accb41d1f344be1181f6
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Device Details

"Zimmer" Longje Eti restricted liner
TW: โ€œๆท้‚โ€้š†ๅ‚‘่‰พๆ้™ๅˆถๅž‹่ฅฏๅขŠ
Risk Class 2

Registration Details

49ab046ae437accb41d1f344be1181f6

DHA05603361701

Company Information

United States

Product Details

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

N Orthopedics

N.3310 Metallic/polymer-like bone cement or cementless cement supplements for restricted hip joints

import

Dates and Status

Apr 26, 2020

Apr 26, 2030